DNA Marker Index data
| Marker Name(s) (separated with a single space) |
Notes |
Identification |
Ancestral7 |
Derived8 |
Chromosome |
Position (hg38)1 |
Position (hg19)2 |
rs1292991583 |
Type: RSID SNP
Position hg183: 10016699
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
G |
3 |
10000015 |
10041699 |
rs1346977541 |
Type: RSID SNP
Position hg183: 101201689
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
T |
3 |
100000155 |
99718999 |
rs1180179840 |
Type: RSID SNP
Position hg183: 10016700
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
TTTG |
3 |
10000016 |
10041700 |
rs1456516895 |
Type: RSID SNP
Position hg183: 10016700
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
G |
3 |
10000016 |
10041700 |
rs1429358195 |
Type: RSID SNP
Position hg183: 10016700
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
TTTGTTG |
T |
3 |
10000016 |
10041700 |
rs1164387808 |
Type: RSID SNP
Position hg183: 10016700
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
TTTG |
T |
3 |
10000016 |
10041700 |
rs1268235579 |
Type: RSID SNP
Position hg183: 101201694
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
3 |
100000160 |
99719004 |
rs1444460045 |
Type: RSID SNP
Position hg183: 101201696
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
G |
3 |
100000162 |
99719006 |
rs934198746 |
Type: RSID SNP
Position hg183: 101201697
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
A |
3 |
100000163 |
99719007 |
rs978017164 |
Type: RSID SNP
Position hg183: 101201596
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
3 |
100000062 |
99718906 |
