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rs41555814

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41555814(C;C)
Make rs41555814(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271131
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41555814
ebirs41555814
HLIrs41555814
Exacrs41555814
Varsomers41555814
Maprs41555814
PheGenIrs41555814
hapmaprs41555814
1000 genomesrs41555814
hgdprs41555814
ensemblrs41555814
gopubmedrs41555814
geneviewrs41555814
scholarrs41555814
googlers41555814
pharmgkbrs41555814
gwascentralrs41555814
openSNPrs41555814
23andMers41555814
23andMe allrs41555814
SNP Nexus

SNPshotrs41555814
SNPdbers41555814
MSV3drs41555814
GWAS Ctlgrs41555814
Max Magnitude0
ClinVar
Risk rs41555814(C,T;C,T)
Alt rs41555814(C,T;C,T)
Reference rs41555814(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238908C>A; NC_000006.11:g.31238908C>G
CLNSRC
CLNACC