DNA Marker Index data
| Marker Name(s) (separated with a single space) |
Notes |
Identification |
Ancestral7 |
Derived8 |
Chromosome |
Position (hg38)1 |
Position (hg19)2 |
rs879233578 |
Type: RSID SNP
Position hg183: 10
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
M |
10 |
10 |
rs201906571 |
Type: RSID SNP
Position hg183: 10008
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
M |
10007 |
10008 |
rs121434476 |
Type: RSID SNP
Position hg183: 10011
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
M |
10010 |
10011 |
rs28374827 |
Type: RSID SNP
Position hg183: 10016
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
A |
M |
10015 |
10016 |
rs879047008 |
Type: RSID SNP
Position hg183: 10031
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
M |
10030 |
10031 |
rs200048690 |
Type: RSID SNP
Position hg183: 10032
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
M |
10031 |
10032 |
rs41347846 |
Type: RSID SNP
Position hg183: 10035
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
A,C,G |
M |
10034 |
10035 |
rs878889554 |
Type: RSID SNP
Position hg183: 10036
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
M |
10035 |
10036 |
rs41362547 |
Type: RSID SNP
Position hg183: 10045
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
M |
10044 |
10045 |
rs876661357 |
Type: RSID SNP
Position hg183: 10047
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
M |
10046 |
10047 |
rs878957961 |
Type: RSID SNP
Position hg183: 10049
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
M |
10048 |
10049 |
rs111033179 |
Type: RSID SNP
Position hg183: 1007
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
M |
1005 |
1007 |
rs371323922 |
Type: RSID SNP
Position hg183: 10053
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
T |
M |
10052 |
10053 |
rs111033213 |
Type: RSID SNP
Position hg183: 1009
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
M |
1007 |
1009 |
rs727504505 |
Type: RSID SNP
Position hg183: 1010
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
M |
1008 |
1010 |
rs41487950 |
Type: RSID SNP
Position hg183: 10085
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
M |
10084 |
10085 |
rs28358274 |
Type: RSID SNP
Position hg183: 10087
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
C,G,T |
M |
10086 |
10087 |
rs879734442 |
Type: RSID SNP
Position hg183: 10115
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
M |
10114 |
10115 |
rs3899188 |
Type: RSID SNP
Position hg183: 10116
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
M |
10115 |
10116 |
rs878916424 |
Type: RSID SNP
Position hg183: 10119
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
M |
10118 |
10119 |