DNA Marker Index data

Marker Name(s) Notes Identification Ancestral7 Derived8 Chromosome Position (hg38)1 Position (hg19)2
rs1164770265
Type: RSID SNP
Position hg183: -not mapped-
NIH DBSNP b153 GRCh38p12 ClinVar?
G
A,T
21
10000065
10478093
rs1276734409
Type: RSID SNP
Position hg183: -not mapped-
NIH DBSNP b153 GRCh38p12 ClinVar?
C
A,T
21
10000066
10478094
rs1450818488
Type: RSID SNP
Position hg183: -not mapped-
NIH DBSNP b153 GRCh38p12 ClinVar?
A
G
21
10000067
10478095
rs1486806369
Type: RSID SNP
Position hg183: -not mapped-
NIH DBSNP b153 GRCh38p12 ClinVar?
T
C
21
10000068
10478096
rs1245642462
Type: RSID SNP
Position hg183: -not mapped-
NIH DBSNP b153 GRCh38p12 ClinVar?
G
A
21
10000069
10478097
rs1214326989
Type: RSID SNP
Position hg183: -not mapped-
NIH DBSNP b153 GRCh38p12 ClinVar?
A
T
21
10000070
10478098
rs1211631673
Type: RSID SNP
Position hg183: -not mapped-
NIH DBSNP b153 GRCh38p12 ClinVar?
G
C
21
10000074
10478102
rs545136239
Type: RSID SNP
Position hg183: -not mapped-
NIH DBSNP b153 GRCh38p12 ClinVar?
T
C
21
10000077
10478105
rs1291107910
Type: RSID SNP
Position hg183: -not mapped-
NIH DBSNP b153 GRCh38p12 ClinVar?
ATTAATC
A
21
10000080
10478108
rs1262610893
Type: RSID SNP
Position hg183: -not mapped-
NIH DBSNP b153 GRCh38p12 ClinVar?
T
C
21
10000081
10478109
rs564930528
Type: RSID SNP
Position hg183: -not mapped-
NIH DBSNP b153 GRCh38p12 ClinVar?
T
A,C
21
10000082
10478110
rs1195966686
Type: RSID SNP
Position hg183: -not mapped-
NIH DBSNP b153 GRCh38p12 ClinVar?
A
G
21
10000083
10478111
rs1212015615
Type: RSID SNP
Position hg183: -not mapped-
NIH DBSNP b153 GRCh38p12 ClinVar?
C
T
21
10000086
10478114
rs1374204080
Type: RSID SNP
Position hg183: -not mapped-
NIH DBSNP b153 GRCh38p12 ClinVar?
TTAAGA
T
21
10000087
10478115
rs1477901471
Type: RSID SNP
Position hg183: -not mapped-
NIH DBSNP b153 GRCh38p12 ClinVar?
GATAAT
G
21
10000091
10478119
rs1171230032
Type: RSID SNP
Position hg183: -not mapped-
NIH DBSNP b153 GRCh38p12 ClinVar?
A
T
21
10000092
10478120
rs1422591454
Type: RSID SNP
Position hg183: -not mapped-
NIH DBSNP b153 GRCh38p12 ClinVar?
T
C
21
10000093
10478121
rs1436221897
Type: RSID SNP
Position hg183: -not mapped-
NIH DBSNP b153 GRCh38p12 ClinVar?
T
C
21
10000098
10478126
rs1312913859
Type: RSID SNP
Position hg183: -not mapped-
NIH DBSNP b153 GRCh38p12 ClinVar?
A
G
21
10000099
10478127
rs1359363839
Type: RSID SNP
Position hg183: -not mapped-
NIH DBSNP b153 GRCh38p12 ClinVar?
G
A
21
10000101
10478129

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