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rs41557317

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41557317(C;T)
Make rs41557317(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271455
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41557317
ebirs41557317
HLIrs41557317
Exacrs41557317
Varsomers41557317
Maprs41557317
PheGenIrs41557317
hapmaprs41557317
1000 genomesrs41557317
hgdprs41557317
ensemblrs41557317
gopubmedrs41557317
geneviewrs41557317
scholarrs41557317
googlers41557317
pharmgkbrs41557317
gwascentralrs41557317
openSNPrs41557317
23andMers41557317
23andMe allrs41557317
SNP Nexus

SNPshotrs41557317
SNPdbers41557317
MSV3drs41557317
GWAS Ctlgrs41557317
GMAF0.02617
Max Magnitude0
ClinVar
Risk rs41557317(T;T)
Alt rs41557317(T;T)
Reference rs41557317(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239232G>A
CLNSRC
CLNACC