Have questions? Visit https://www.reddit.com/r/SNPedia

rs9260172

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs9260172(C;T)
Make rs9260172(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944116
GeneHLA-A
is asnp
is mentioned by
dbSNPrs9260172
ebirs9260172
HLIrs9260172
Exacrs9260172
Varsomers9260172
Maprs9260172
PheGenIrs9260172
hapmaprs9260172
1000 genomesrs9260172
hgdprs9260172
ensemblrs9260172
gopubmedrs9260172
geneviewrs9260172
scholarrs9260172
googlers9260172
pharmgkbrs9260172
gwascentralrs9260172
openSNPrs9260172
23andMers9260172
23andMe allrs9260172
SNP Nexus

SNPshotrs9260172
SNPdbers9260172
MSV3drs9260172
GWAS Ctlgrs9260172
Max Magnitude0
ClinVar
Risk rs9260172(T;T)
Alt rs9260172(T;T)
Reference rs9260172(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911893C>T
CLNSRC
CLNACC