DNA Marker Index data
| Marker Name(s) (separated with a single space) |
Notes |
Identification |
Ancestral7 |
Derived8 |
Chromosome |
Position (hg38)1 |
Position (hg19)2 |
rs1247046355 |
Type: RSID SNP
Position hg183: 98918114
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
12 |
100000205 |
100393983 |
rs916592887 |
Type: RSID SNP
Position hg183: 98918125
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
12 |
100000216 |
100393994 |
rs556927712 |
Type: RSID SNP
Position hg183: 98918132
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
12 |
100000223 |
100394001 |
rs189537102 |
Type: RSID SNP
Position hg183: 98918133
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
12 |
100000224 |
100394002 |
rs188192095 |
Type: RSID SNP
Position hg183: 10043889
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
12 |
10000023 |
10152622 |
rs1046465928 |
Type: RSID SNP
Position hg183: 98918145
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
12 |
100000236 |
100394014 |
rs909208066 |
Type: RSID SNP
Position hg183: 98918149
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
12 |
100000240 |
100394018 |
rs938026167 |
Type: RSID SNP
Position hg183: 98918154
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
12 |
100000245 |
100394023 |
rs565775179 |
Type: RSID SNP
Position hg183: 10043891
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
12 |
10000025 |
10152624 |
rs375984525 |
Type: RSID SNP
Position hg183: 98918021
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
TTTTG |
T |
12 |
100000112 |
100393890 |
rs558193491 |
Type: RSID SNP
Position hg183: 98918021
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
TTTTG |
T |
12 |
100000112 |
100393890 |
rs1302795664 |
Type: RSID SNP
Position hg183: 98918014
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
12 |
100000105 |
100393883 |
rs1430674325 |
Type: RSID SNP
Position hg183: 98918013
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
T |
12 |
100000104 |
100393882 |
rs1387028743 |
Type: RSID SNP
Position hg183: 10043876
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
A |
12 |
10000010 |
10152609 |
rs1260002036 |
Type: RSID SNP
Position hg183: 98918008
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
CT |
C |
12 |
100000099 |
100393877 |
rs1342910211 |
Type: RSID SNP
Position hg183: 98918003
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
A |
12 |
100000094 |
100393872 |
rs1230526724 |
Type: RSID SNP
Position hg183: 98917999
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
12 |
100000090 |
100393868 |
rs1436141367 |
Type: RSID SNP
Position hg183: 98917997
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
12 |
100000088 |
100393866 |
rs138317906 |
Type: RSID SNP
Position hg183: 98917995
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
12 |
100000086 |
100393864 |
rs978632960 |
Type: RSID SNP
Position hg183: 98917984
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
12 |
100000075 |
100393853 |