DNA Marker Index data

Marker Name(s) 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
rs760315250
Type: RSID SNP
Position hg183: 10449242
NIH DBSNP b153 GRCh38p12 ClinVar?
T
A
Y
10001633
9839242
rs1317007873
Type: RSID SNP
Position hg183: 10449246
NIH DBSNP b153 GRCh38p12 ClinVar?
GT
G
Y
10001637
9839246
rs763722212
Type: RSID SNP
Position hg183: 10449343
NIH DBSNP b153 GRCh38p12 ClinVar?
A
G
Y
10001734
9839343
rs753361310
Type: RSID SNP
Position hg183: 10449409
NIH DBSNP b153 GRCh38p12 ClinVar?
G
A
Y
10001800
9839409
rs757788147
Type: RSID SNP
Position hg183: 10449478
NIH DBSNP b153 GRCh38p12 ClinVar?
A
G
Y
10001869
9839478
rs1217370806
Type: RSID SNP
Position hg183: 10449545
NIH DBSNP b153 GRCh38p12 ClinVar?
CA
C
Y
10001936
9839545
rs576187716
Type: RSID SNP
Position hg183: 10449666
NIH DBSNP b153 GRCh38p12 ClinVar?
G
T
Y
10002057
9839666
rs113643038
Type: RSID SNP
Position hg183: 10449719
NIH DBSNP b153 GRCh38p12 ClinVar?
T
C
Y
10002110
9839719
rs1322442072
Type: RSID SNP
Position hg183: 10449878
NIH DBSNP b153 GRCh38p12 ClinVar?
C
A
Y
10002269
9839878
rs1270699425
Type: RSID SNP
Position hg183: 10449932
NIH DBSNP b153 GRCh38p12 ClinVar?
C
A
Y
10002323
9839932

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