DNA Marker Index data

Marker Name(s) Notes Identification Ancestral7 Derived8 Chromosome Position (hg38)1 Position (hg19)2
rs894831941
Type: RSID SNP
Position hg183: 9844043
NIH DBSNP b153 GRCh38p12 ClinVar?
C
T
17
10000001
9903318
rs973399740
Type: RSID SNP
Position hg183: 9844044
NIH DBSNP b153 GRCh38p12 ClinVar?
G
A
17
10000002
9903319
rs1445930213
Type: RSID SNP
Position hg183: 9844045
NIH DBSNP b153 GRCh38p12 ClinVar?
T
A
17
10000003
9903320
rs1258976558
Type: RSID SNP
Position hg183: 9844048
NIH DBSNP b153 GRCh38p12 ClinVar?
G
A
17
10000006
9903323
rs917423623
Type: RSID SNP
Position hg183: 9844050
NIH DBSNP b153 GRCh38p12 ClinVar?
G
A
17
10000008
9903325
rs563665304
Type: RSID SNP
Position hg183: 9844051
NIH DBSNP b153 GRCh38p12 ClinVar?
C
T
17
10000009
9903326
rs1044443503
Type: RSID SNP
Position hg183: 9844052
NIH DBSNP b153 GRCh38p12 ClinVar?
G
A
17
10000010
9903327
rs927404198
Type: RSID SNP
Position hg183: 9844054
NIH DBSNP b153 GRCh38p12 ClinVar?
A
G
17
10000012
9903329
rs1055190296
Type: RSID SNP
Position hg183: 849992
NIH DBSNP b153 GRCh38p12 ClinVar?
C
T
17
1000002
903242
rs1221430474
Type: RSID SNP
Position hg183: 9844062
NIH DBSNP b153 GRCh38p12 ClinVar?
C
G
17
10000020
9903337
rs936104222
Type: RSID SNP
Position hg183: 9844071
NIH DBSNP b153 GRCh38p12 ClinVar?
G
T
17
10000029
9903346
rs1321751652
Type: RSID SNP
Position hg183: 9844073
NIH DBSNP b153 GRCh38p12 ClinVar?
C
A
17
10000031
9903348
rs1054355470
Type: RSID SNP
Position hg183: 9844080
NIH DBSNP b153 GRCh38p12 ClinVar?
A
C
17
10000038
9903355
rs761604863
Type: RSID SNP
Position hg183: 9844083
NIH DBSNP b153 GRCh38p12 ClinVar?
C
CA
17
10000041
9903358
rs112874387
Type: RSID SNP
Position hg183: 9844083
NIH DBSNP b153 GRCh38p12 ClinVar?
CA
C
17
10000041
9903358
rs1325931945
Type: RSID SNP
Position hg183: 9844087
NIH DBSNP b153 GRCh38p12 ClinVar?
T
C
17
10000045
9903362
rs764493772
Type: RSID SNP
Position hg183: 9844089
NIH DBSNP b153 GRCh38p12 ClinVar?
G
A
17
10000047
9903364
rs1384475102
Type: RSID SNP
Position hg183: 9844094
NIH DBSNP b153 GRCh38p12 ClinVar?
T
C
17
10000052
9903369
rs1389982709
Type: RSID SNP
Position hg183: 9844097
NIH DBSNP b153 GRCh38p12 ClinVar?
T
C
17
10000055
9903372
rs1336565049
Type: RSID SNP
Position hg183: 9844099
NIH DBSNP b153 GRCh38p12 ClinVar?
G
A
17
10000057
9903374

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