DNA Marker Index data

Marker Name(s) Notes Identification Ancestral7 Derived8 Chromosome Position (hg38)1 Position (hg19)2
rs1468373888
 Type: RSID SNP
Position hg183: 51000 		NIH DBSNP b153 GRCh38p12 ClinVar?
G
T
19
 100000
100000
rs769522595
 Type: RSID SNP
Position hg183: 950999 		NIH DBSNP b153 GRCh38p12 ClinVar?
A
G
19
 1000000
999999
rs1037395275
 Type: RSID SNP
Position hg183: 9971678 		NIH DBSNP b153 GRCh38p12 ClinVar?
C
A
19
 10000002
10110678
rs897606705
 Type: RSID SNP
Position hg183: 9971681 		NIH DBSNP b153 GRCh38p12 ClinVar?
G
A
19
 10000005
10110681
rs1344673050
 Type: RSID SNP
Position hg183: 9971685 		NIH DBSNP b153 GRCh38p12 ClinVar?
C
T
19
 10000009
10110685
rs1238870071
 Type: RSID SNP
Position hg183: 951000 		NIH DBSNP b153 GRCh38p12 ClinVar?
C
T
19
 1000001
1000000
rs188767851
 Type: RSID SNP
Position hg183: 9971687 		NIH DBSNP b153 GRCh38p12 ClinVar?
A
G
19
 10000011
10110687
rs893846567
 Type: RSID SNP
Position hg183: 9971692 		NIH DBSNP b153 GRCh38p12 ClinVar?
C
A
19
 10000016
10110692
rs1278355202
 Type: RSID SNP
Position hg183: 9971693 		NIH DBSNP b153 GRCh38p12 ClinVar?
C
A
19
 10000017
10110693
rs1025772833
 Type: RSID SNP
Position hg183: 9971694 		NIH DBSNP b153 GRCh38p12 ClinVar?
A
T
19
 10000018
10110694
rs1236007119
 Type: RSID SNP
Position hg183: 9971695 		NIH DBSNP b153 GRCh38p12 ClinVar?
A
C
19
 10000019
10110695
rs1315894918
 Type: RSID SNP
Position hg183: 951001 		NIH DBSNP b153 GRCh38p12 ClinVar?
G
A
19
 1000002
1000001
rs1010936033
 Type: RSID SNP
Position hg183: 9971704 		NIH DBSNP b153 GRCh38p12 ClinVar?
G
A
19
 10000028
10110704
rs1301414551
 Type: RSID SNP
Position hg183: 9971717 		NIH DBSNP b153 GRCh38p12 ClinVar?
A
ATCTG
19
 10000041
10110717
rs1445403652
 Type: RSID SNP
Position hg183: 9971720 		NIH DBSNP b153 GRCh38p12 ClinVar?
C
CTATAGGTGATT
19
 10000044
10110720
rs1397749066
 Type: RSID SNP
Position hg183: 9971721 		NIH DBSNP b153 GRCh38p12 ClinVar?
AC
A
19
 10000045
10110721
rs1332887008
 Type: RSID SNP
Position hg183: 9971723 		NIH DBSNP b153 GRCh38p12 ClinVar?
C
T
19
 10000047
10110723
rs1307283728
 Type: RSID SNP
Position hg183: 951004 		NIH DBSNP b153 GRCh38p12 ClinVar?
C
G
19
 1000005
1000004
rs1018780997
 Type: RSID SNP
Position hg183: 9971727 		NIH DBSNP b153 GRCh38p12 ClinVar?
C
A,T
19
 10000051
10110727
rs1216428123
 Type: RSID SNP
Position hg183: 9971731 		NIH DBSNP b153 GRCh38p12 ClinVar?
G
C
19
 10000055
10110731

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