DNA Marker Index data
| Marker Name(s) (separated with a single space) |
Notes |
Identification |
Ancestral7 |
Derived8 |
Chromosome |
Position (hg38)1 |
Position (hg19)2 |
rs1405105418 |
Type: RSID SNP
Position hg183: 101201615
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
3 |
100000081 |
99718925 |
rs925939700 |
Type: RSID SNP
Position hg183: 101201621
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
A |
3 |
100000087 |
99718931 |
rs1315942225 |
Type: RSID SNP
Position hg183: 101201623
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
3 |
100000089 |
99718933 |
rs1396645629 |
Type: RSID SNP
Position hg183: 101201625
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C,G |
3 |
100000091 |
99718935 |
rs1408579658 |
Type: RSID SNP
Position hg183: 101201626
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
3 |
100000092 |
99718936 |
rs544183788 |
Type: RSID SNP
Position hg183: 101201627
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
3 |
100000093 |
99718937 |
rs925073767 |
Type: RSID SNP
Position hg183: 101201628
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
3 |
100000094 |
99718938 |
rs1473623702 |
Type: RSID SNP
Position hg183: 101201632
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
A |
3 |
100000098 |
99718942 |
rs936494078 |
Type: RSID SNP
Position hg183: 101201639
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
3 |
100000105 |
99718949 |
rs990693245 |
Type: RSID SNP
Position hg183: 101201642
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
3 |
100000108 |
99718952 |
rs1366846146 |
Type: RSID SNP
Position hg183: 10016695
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
3 |
10000011 |
10041695 |
rs754856384 |
Type: RSID SNP
Position hg183: 101201644
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
T |
3 |
100000110 |
99718954 |
rs948862324 |
Type: RSID SNP
Position hg183: 101201652
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
3 |
100000118 |
99718962 |
rs1214052124 |
Type: RSID SNP
Position hg183: 101201654
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
3 |
100000120 |
99718964 |
rs1446744441 |
Type: RSID SNP
Position hg183: 101201665
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
3 |
100000131 |
99718975 |
rs1285600577 |
Type: RSID SNP
Position hg183: 101201668
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
T |
3 |
100000134 |
99718978 |
rs1348271468 |
Type: RSID SNP
Position hg183: 101201669
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
3 |
100000135 |
99718979 |
rs1320801063 |
Type: RSID SNP
Position hg183: 101201677
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
A |
3 |
100000143 |
99718987 |
rs922666497 |
Type: RSID SNP
Position hg183: 101201682
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
3 |
100000148 |
99718992 |
rs1223806009 |
Type: RSID SNP
Position hg183: 101201683
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
3 |
100000149 |
99718993 |