DNA Marker Index data
| Marker Name(s) (separated with a single space) |
Notes |
Identification |
Ancestral7 |
Derived8 |
Chromosome |
Position (hg38)1 |
Position (hg19)2 |
rs562872356 |
Type: RSID SNP
Position hg183: 9928814
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
G |
20 |
10000166 |
9980814 |
rs549021115 |
Type: RSID SNP
Position hg183: 928660
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
20 |
1000017 |
980660 |
rs1297483809 |
Type: RSID SNP
Position hg183: 9928823
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
T |
20 |
10000175 |
9980823 |
rs1261530046 |
Type: RSID SNP
Position hg183: 9928825
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
20 |
10000177 |
9980825 |
rs537190620 |
Type: RSID SNP
Position hg183: 928661
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
20 |
1000018 |
980661 |
rs1192449723 |
Type: RSID SNP
Position hg183: 9928828
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
20 |
10000180 |
9980828 |
rs1339995033 |
Type: RSID SNP
Position hg183: 9928832
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
A |
20 |
10000184 |
9980832 |
rs1215276126 |
Type: RSID SNP
Position hg183: 9928837
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
20 |
10000189 |
9980837 |
rs909244387 |
Type: RSID SNP
Position hg183: 9928849
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
20 |
10000201 |
9980849 |
rs1285944522 |
Type: RSID SNP
Position hg183: 9928853
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
20 |
10000205 |
9980853 |
