DNA Marker Index data

Marker Name(s) Notes Identification Ancestral7 Derived8 Chromosome Position (hg38)1 Position (hg19)2
rs1429791606
 Type: RSID SNP
Position hg183: 10001550 		NIH DBSNP b153 GRCh38p12 ClinVar?
C
T
16
 10000192
10094049
rs759726529
 Type: RSID SNP
Position hg183: 10001552 		NIH DBSNP b153 GRCh38p12 ClinVar?
C
G,T
16
 10000194
10094051
rs903371230
 Type: RSID SNP
Position hg183: 10001555 		NIH DBSNP b153 GRCh38p12 ClinVar?
T
A
16
 10000197
10094054
rs1320003953
 Type: RSID SNP
Position hg183: 10001558 		NIH DBSNP b153 GRCh38p12 ClinVar?
T
C
16
 10000200
10094057
rs1459063615
 Type: RSID SNP
Position hg183: 10001563 		NIH DBSNP b153 GRCh38p12 ClinVar?
T
C
16
 10000205
10094062
rs547982916
 Type: RSID SNP
Position hg183: 10001565 		NIH DBSNP b153 GRCh38p12 ClinVar?
T
C
16
 10000207
10094064
rs1351789692
 Type: RSID SNP
Position hg183: 10001569 		NIH DBSNP b153 GRCh38p12 ClinVar?
T
C
16
 10000211
10094068
rs1216115621
 Type: RSID SNP
Position hg183: 10001595 		NIH DBSNP b153 GRCh38p12 ClinVar?
G
T
16
 10000237
10094094
rs1056732479
 Type: RSID SNP
Position hg183: 990025 		NIH DBSNP b153 GRCh38p12 ClinVar?
C
A,T
16
 1000024
1050024
rs1480224122
 Type: RSID SNP
Position hg183: 89999 		NIH DBSNP b153 GRCh38p12 ClinVar?
G
A
16
 100001
149999
rs148607663
 Type: RSID SNP
Position hg183: 10001451 		NIH DBSNP b153 GRCh38p12 ClinVar?
C
T
16
 10000093
10093950
rs1298000609
 Type: RSID SNP
Position hg183: 10001449 		NIH DBSNP b153 GRCh38p12 ClinVar?
C
T
16
 10000091
10093948
rs1016063312
 Type: RSID SNP
Position hg183: 10001448 		NIH DBSNP b153 GRCh38p12 ClinVar?
C
A,T
16
 10000090
10093947
rs773514182
 Type: RSID SNP
Position hg183: 990010 		NIH DBSNP b153 GRCh38p12 ClinVar?
A
T
16
 1000009
1050009
rs1418639754
 Type: RSID SNP
Position hg183: 10001445 		NIH DBSNP b153 GRCh38p12 ClinVar?
C
CT
16
 10000087
10093944
rs1292632509
 Type: RSID SNP
Position hg183: 10001445 		NIH DBSNP b153 GRCh38p12 ClinVar?
C
T
16
 10000087
10093944
rs147173559
 Type: RSID SNP
Position hg183: 10001440 		NIH DBSNP b153 GRCh38p12 ClinVar?
A
T
16
 10000082
10093939
rs189275130
 Type: RSID SNP
Position hg183: 10001434 		NIH DBSNP b153 GRCh38p12 ClinVar?
C
T
16
 10000076
10093933
rs1240579553
 Type: RSID SNP
Position hg183: 10001429 		NIH DBSNP b153 GRCh38p12 ClinVar?
C
T
16
 10000071
10093928
rs999500399
 Type: RSID SNP
Position hg183: 10001424 		NIH DBSNP b153 GRCh38p12 ClinVar?
T
G
16
 10000066
10093923

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