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rs41557122

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41557122(C;G)
Make rs41557122(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943510
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41557122
ebirs41557122
HLIrs41557122
Exacrs41557122
Varsomers41557122
Maprs41557122
PheGenIrs41557122
hapmaprs41557122
1000 genomesrs41557122
hgdprs41557122
ensemblrs41557122
gopubmedrs41557122
geneviewrs41557122
scholarrs41557122
googlers41557122
pharmgkbrs41557122
gwascentralrs41557122
openSNPrs41557122
23andMers41557122
23andMe allrs41557122
SNP Nexus

SNPshotrs41557122
SNPdbers41557122
MSV3drs41557122
GWAS Ctlgrs41557122
Max Magnitude0
ClinVar
Risk rs41557122(G,T;G,T)
Alt rs41557122(G,T;G,T)
Reference rs41557122(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911287C>G; NC_000006.11:g.29911287C>T
CLNSRC
CLNACC