DNA Marker Index data
| Marker Name(s) (separated with a single space) |
Notes |
Identification |
Ancestral7 |
Derived8 |
Chromosome |
Position (hg38)1 |
Position (hg19)2 |
rs776640529 |
Type: RSID SNP
Position hg183: 10447803
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
Y |
10000194 |
9837803 |
rs1305797750 |
Type: RSID SNP
Position hg183: 10447944
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
Y |
10000335 |
9837944 |
rs762908117 |
Type: RSID SNP
Position hg183: 10448078
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
Y |
10000469 |
9838078 |
rs770703600 |
Type: RSID SNP
Position hg183: 10448180
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
C |
Y |
10000571 |
9838180 |
rs774207324 |
Type: RSID SNP
Position hg183: 10448194
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
Y |
10000585 |
9838194 |
rs35956254 |
Type: RSID SNP
Position hg183: 10448581
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
TG |
Y |
10000972 |
9838581 |
rs367700933 |
Type: RSID SNP
Position hg183: 10448684
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
Y |
10001075 |
9838684 |
rs759234596 |
Type: RSID SNP
Position hg183: 10448737
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
Y |
10001128 |
9838737 |
rs767264252 |
Type: RSID SNP
Position hg183: 10448822
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
C |
Y |
10001213 |
9838822 |
rs752370353 |
Type: RSID SNP
Position hg183: 10449227
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
Y |
10001618 |
9839227 |
