DNA Marker Index data
| Marker Name(s) (separated with a single space) |
Notes |
Identification |
Ancestral7 |
Derived8 |
Chromosome |
Position (hg38)1 |
Position (hg19)2 |
rs971100399 |
Type: RSID SNP
Position hg183: 10057601
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
2 |
10000022 |
10140150 |
rs372893192 |
Type: RSID SNP
Position hg183: 99983114
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
AGCTCAAATCTTGTTGATTTAGT |
A |
2 |
100000220 |
100616682 |
rs764589147 |
Type: RSID SNP
Position hg183: 10057602
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
2 |
10000023 |
10140151 |
rs1468647721 |
Type: RSID SNP
Position hg183: 99983126
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
GTTGA |
G |
2 |
100000232 |
100616694 |
rs1158026643 |
Type: RSID SNP
Position hg183: 99983127
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
G |
2 |
100000233 |
100616695 |
rs1271842318 |
Type: RSID SNP
Position hg183: 99983131
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
2 |
100000237 |
100616699 |
rs1431475207 |
Type: RSID SNP
Position hg183: 99983132
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
G |
2 |
100000238 |
100616700 |
rs1428667423 |
Type: RSID SNP
Position hg183: 99983133
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
2 |
100000239 |
100616701 |
rs1281947359 |
Type: RSID SNP
Position hg183: 10057603
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
2 |
10000024 |
10140152 |
rs1400758185 |
Type: RSID SNP
Position hg183: 99982992
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
2 |
100000098 |
100616560 |
rs1222762859 |
Type: RSID SNP
Position hg183: 99982987
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
2 |
100000093 |
100616555 |
rs1324646665 |
Type: RSID SNP
Position hg183: 99982985
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
2 |
100000091 |
100616553 |
rs1347886450 |
Type: RSID SNP
Position hg183: 99982983
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
CAT |
C |
2 |
100000089 |
100616551 |
rs1010819548 |
Type: RSID SNP
Position hg183: 99982983
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
G |
2 |
100000089 |
100616551 |
rs893166817 |
Type: RSID SNP
Position hg183: 99982965
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
G |
2 |
100000071 |
100616533 |
rs1347160454 |
Type: RSID SNP
Position hg183: 99982964
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
2 |
100000070 |
100616532 |
rs1050437031 |
Type: RSID SNP
Position hg183: 99982962
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
2 |
100000068 |
100616530 |
rs533999951 |
Type: RSID SNP
Position hg183: 99982960
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G,T |
2 |
100000066 |
100616528 |
rs996150884 |
Type: RSID SNP
Position hg183: 99982956
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
2 |
100000062 |
100616524 |
rs565564265 |
Type: RSID SNP
Position hg183: 99982952
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
2 |
100000058 |
100616520 |