DNA Marker Index data
| Marker Name(s) (separated with a single space) |
Notes |
Identification |
Ancestral7 |
Derived8 |
Chromosome |
Position (hg38)1 |
Position (hg19)2 |
rs1297590116 |
Type: RSID SNP
Position hg183: 99450261
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G |
13 |
100000006 |
100652260 |
rs1416239449 |
Type: RSID SNP
Position hg183: 99450262
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
G,T |
13 |
100000007 |
100652261 |
rs1310678575 |
Type: RSID SNP
Position hg183: 99450267
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
13 |
100000012 |
100652266 |
rs2390330 |
Type: RSID SNP
Position hg183: 99450271
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
13 |
100000016 |
100652270 |
rs918988339 |
Type: RSID SNP
Position hg183: 99450278
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
13 |
100000023 |
100652277 |
rs930399990 |
Type: RSID SNP
Position hg183: 99450284
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
13 |
100000029 |
100652283 |
rs1375174896 |
Type: RSID SNP
Position hg183: 99450285
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
A |
13 |
100000030 |
100652284 |
rs933418180 |
Type: RSID SNP
Position hg183: 99450289
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
13 |
100000034 |
100652288 |
rs1048687211 |
Type: RSID SNP
Position hg183: 99450299
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
13 |
100000044 |
100652298 |
rs1358868178 |
Type: RSID SNP
Position hg183: 99450302
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
13 |
100000047 |
100652301 |
rs894136094 |
Type: RSID SNP
Position hg183: 99450305
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
13 |
100000050 |
100652304 |
rs1442916158 |
Type: RSID SNP
Position hg183: 99450306
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
13 |
100000051 |
100652305 |
rs1303671910 |
Type: RSID SNP
Position hg183: 99450308
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
13 |
100000053 |
100652307 |
rs1421643089 |
Type: RSID SNP
Position hg183: 99450311
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
13 |
100000056 |
100652310 |
rs1369714248 |
Type: RSID SNP
Position hg183: 99450311
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
GCCACCATGC |
G |
13 |
100000056 |
100652310 |
rs948615734 |
Type: RSID SNP
Position hg183: 99450340
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
G |
13 |
100000085 |
100652339 |
rs1159207449 |
Type: RSID SNP
Position hg183: 99450344
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
T |
C |
13 |
100000089 |
100652343 |
rs1438793744 |
Type: RSID SNP
Position hg183: 99450347
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
A |
T |
13 |
100000092 |
100652346 |
rs551924130 |
Type: RSID SNP
Position hg183: 99450350
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
C |
T |
13 |
100000095 |
100652349 |
rs547389624 |
Type: RSID SNP
Position hg183: 99450351
|
NIH DBSNP b153 GRCh38p12 ClinVar?
|
G |
A |
13 |
100000096 |
100652350 |