DNA Marker Index data

Marker Name(s) Notes Identification Ancestral7 Derived8 Chromosome Position (hg38)1 Position (hg19)2
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
rs1297753942
Type: RSID SNP
Position hg183: 9928857
NIH DBSNP b153 GRCh38p12 ClinVar?
C
A
20
10000209
9980857
rs73895890
Type: RSID SNP
Position hg183: 9928858
NIH DBSNP b153 GRCh38p12 ClinVar?
C
T
20
10000210
9980858
rs1343696383
Type: RSID SNP
Position hg183: 9928861
NIH DBSNP b153 GRCh38p12 ClinVar?
T
C
20
10000213
9980861
rs6133773
Type: RSID SNP
Position hg183: 9928865
NIH DBSNP b153 GRCh38p12 ClinVar?
C
T
20
10000217
9980865
rs1231444385
Type: RSID SNP
Position hg183: 928655
NIH DBSNP b153 GRCh38p12 ClinVar?
G
T
20
1000012
980655
rs1422363675
Type: RSID SNP
Position hg183: 9928767
NIH DBSNP b153 GRCh38p12 ClinVar?
C
A
20
10000119
9980767
rs1230460758
Type: RSID SNP
Position hg183: 9928765
NIH DBSNP b153 GRCh38p12 ClinVar?
A
AC
20
10000117
9980765
rs1013608274
Type: RSID SNP
Position hg183: 9928760
NIH DBSNP b153 GRCh38p12 ClinVar?
G
A
20
10000112
9980760
rs964480190
Type: RSID SNP
Position hg183: 9928757
NIH DBSNP b153 GRCh38p12 ClinVar?
GGAGA
G
20
10000109
9980757
rs1215527393
Type: RSID SNP
Position hg183: 9928756
NIH DBSNP b153 GRCh38p12 ClinVar?
T
C
20
10000108
9980756
rs1283422665
Type: RSID SNP
Position hg183: 9928753
NIH DBSNP b153 GRCh38p12 ClinVar?
A
G
20
10000105
9980753

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