DNA Marker Index data
| Marker Name(s) (separated with a single space) |
Notes |
Identification |
Ancestral7 |
Derived8 |
Chromosome |
Position (hg38)1 |
Position (hg19)2 |
rs138880521 |
Type: RSID SNP
Position hg183: 101749969
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
10 |
100000222 |
101759979 |
rs543806515 |
Type: RSID SNP
Position hg183: 101749971
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
10 |
100000224 |
101759981 |
rs973920304 |
Type: RSID SNP
Position hg183: 101749973
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
10 |
100000226 |
101759983 |
rs767004351 |
Type: RSID SNP
Position hg183: 101749980
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
10 |
100000233 |
101759990 |
rs11596870 |
Type: RSID SNP
Position hg183: 101749982
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
10 |
100000235 |
101759992 |
rs931955548 |
Type: RSID SNP
Position hg183: 101749983
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
T |
10 |
100000236 |
101759993 |
rs1050448952 |
Type: RSID SNP
Position hg183: 101749996
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A,C |
10 |
100000249 |
101760006 |
rs1430960511 |
Type: RSID SNP
Position hg183: 101749998
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
10 |
100000251 |
101760008 |
rs1395813003 |
Type: RSID SNP
Position hg183: 101750009
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
10 |
100000262 |
101760019 |
rs553147263 |
Type: RSID SNP
Position hg183: 101749850
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
A |
10 |
100000103 |
101759860 |
rs534483167 |
Type: RSID SNP
Position hg183: 1035941
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
10 |
1000001 |
1045941 |
rs1363916700 |
Type: RSID SNP
Position hg183: 101749842
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
10 |
100000095 |
101759852 |
rs1033986510 |
Type: RSID SNP
Position hg183: 101749835
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
10 |
100000088 |
101759845 |
rs1299802631 |
Type: RSID SNP
Position hg183: 101749834
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
10 |
100000087 |
101759844 |
rs570059435 |
Type: RSID SNP
Position hg183: 101749828
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
10 |
100000081 |
101759838 |
rs1169795623 |
Type: RSID SNP
Position hg183: 101749823
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
C |
10 |
100000076 |
101759833 |
rs1003206944 |
Type: RSID SNP
Position hg183: 101749822
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
10 |
100000075 |
101759832 |
rs1265817977 |
Type: RSID SNP
Position hg183: 101749814
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
10 |
100000067 |
101759824 |
rs1021307156 |
Type: RSID SNP
Position hg183: 101749810
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
10 |
100000063 |
101759820 |
rs1010370374 |
Type: RSID SNP
Position hg183: 101749801
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
10 |
100000054 |
101759811 |