DNA Marker Index data
| Marker Name(s) (separated with a single space) |
Notes |
Identification |
Ancestral7 |
Derived8 |
Chromosome |
Position (hg38)1 |
Position (hg19)2 |
rs1020265686 |
Type: RSID SNP
Position hg183: 99536286
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
C,G |
14 |
100000196 |
100466533 |
rs561825165 |
Type: RSID SNP
Position hg183: 99536287
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
G |
14 |
100000197 |
100466534 |
rs992555295 |
Type: RSID SNP
Position hg183: 99536288
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
14 |
100000198 |
100466535 |
rs1390282666 |
Type: RSID SNP
Position hg183: 99536299
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
14 |
100000209 |
100466546 |
rs915648324 |
Type: RSID SNP
Position hg183: 99536300
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
14 |
100000210 |
100466547 |
rs948361547 |
Type: RSID SNP
Position hg183: 99536310
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
14 |
100000220 |
100466557 |
rs1248626841 |
Type: RSID SNP
Position hg183: 99536314
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
G |
14 |
100000224 |
100466561 |
rs1467847212 |
Type: RSID SNP
Position hg183: 99536328
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
14 |
100000238 |
100466575 |
rs774930330 |
Type: RSID SNP
Position hg183: 99536331
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
T |
14 |
100000241 |
100466578 |
rs1232965037 |
Type: RSID SNP
Position hg183: 99536212
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
14 |
100000122 |
100466459 |
rs886124640 |
Type: RSID SNP
Position hg183: 99536209
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
C |
14 |
100000119 |
100466456 |
rs1479547287 |
Type: RSID SNP
Position hg183: 99536208
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
TG |
14 |
100000118 |
100466455 |
rs1178661095 |
Type: RSID SNP
Position hg183: 99536199
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
14 |
100000109 |
100466446 |
rs1020126695 |
Type: RSID SNP
Position hg183: 99536194
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
G |
14 |
100000104 |
100466441 |
rs533600235 |
Type: RSID SNP
Position hg183: 99536193
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
G |
14 |
100000103 |
100466440 |
rs1432588007 |
Type: RSID SNP
Position hg183: 99536183
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
G |
14 |
100000093 |
100466430 |
rs1360629790 |
Type: RSID SNP
Position hg183: 99536182
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
G |
14 |
100000092 |
100466429 |
rs1048738652 |
Type: RSID SNP
Position hg183: 99536179
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
14 |
100000089 |
100466426 |
rs1314783917 |
Type: RSID SNP
Position hg183: 99536177
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
14 |
100000087 |
100466424 |
rs1430852397 |
Type: RSID SNP
Position hg183: 99536166
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
14 |
100000076 |
100466413 |