DNA Marker Index data

Marker Name(s) Notes Identification Ancestral7 Derived8 Chromosome Position (hg38)1 Position (hg19)2
rs1189414375
 Type: RSID SNP
Position hg183: -not mapped- 		NIH DBSNP b153 GRCh38p12 ClinVar?
C
T
X
 100000
rs1285725828
 Type: RSID SNP
Position hg183: 99141659 		NIH DBSNP b153 GRCh38p12 ClinVar?
G
T
X
 100000005
99255003
rs1238296025
 Type: RSID SNP
Position hg183: 99141664 		NIH DBSNP b153 GRCh38p12 ClinVar?
TC
T
X
 100000010
99255008
rs767877553
 Type: RSID SNP
Position hg183: 99141667 		NIH DBSNP b153 GRCh38p12 ClinVar?
C
T
X
 100000013
99255011
rs1237126943
 Type: RSID SNP
Position hg183: 9928042 		NIH DBSNP b153 GRCh38p12 ClinVar?
CTTCTAGT
C
X
 10000002
9968042
rs957667030
 Type: RSID SNP
Position hg183: 99141700 		NIH DBSNP b153 GRCh38p12 ClinVar?
G
A
X
 100000046
99255044
rs1395535391
 Type: RSID SNP
Position hg183: 99141707 		NIH DBSNP b153 GRCh38p12 ClinVar?
T
C
X
 100000053
99255051
rs530200528
 Type: RSID SNP
Position hg183: 99141708 		NIH DBSNP b153 GRCh38p12 ClinVar?
G
A
X
 100000054
99255052
rs1467048110
 Type: RSID SNP
Position hg183: 99141710 		NIH DBSNP b153 GRCh38p12 ClinVar?
T
A
X
 100000056
99255054
rs1005497920
 Type: RSID SNP
Position hg183: 99141711 		NIH DBSNP b153 GRCh38p12 ClinVar?
C
T
X
 100000057
99255055
rs1301083016
 Type: RSID SNP
Position hg183: 99141731 		NIH DBSNP b153 GRCh38p12 ClinVar?
T
C
X
 100000077
99255075
rs989375875
 Type: RSID SNP
Position hg183: 99141732 		NIH DBSNP b153 GRCh38p12 ClinVar?
G
A
X
 100000078
99255076
rs1416533318
 Type: RSID SNP
Position hg183: 99141747 		NIH DBSNP b153 GRCh38p12 ClinVar?
G
A
X
 100000093
99255091
rs1375893222
 Type: RSID SNP
Position hg183: 99141760 		NIH DBSNP b153 GRCh38p12 ClinVar?
A
G
X
 100000106
99255104
rs1157798701
 Type: RSID SNP
Position hg183: 99141775 		NIH DBSNP b153 GRCh38p12 ClinVar?
T
C
X
 100000121
99255119
rs1029349401
 Type: RSID SNP
Position hg183: 99141778 		NIH DBSNP b153 GRCh38p12 ClinVar?
A
G
X
 100000124
99255122
rs961690690
 Type: RSID SNP
Position hg183: 99141791 		NIH DBSNP b153 GRCh38p12 ClinVar?
A
C
X
 100000137
99255135
rs112795980
 Type: RSID SNP
Position hg183: 99141793 		NIH DBSNP b153 GRCh38p12 ClinVar?
T
C
X
 100000139
99255137
rs1422733883
 Type: RSID SNP
Position hg183: 99141799 		NIH DBSNP b153 GRCh38p12 ClinVar?
A
G
X
 100000145
99255143
rs1253460145
 Type: RSID SNP
Position hg183: 99141802 		NIH DBSNP b153 GRCh38p12 ClinVar?
G
C
X
 100000148
99255146

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