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rs41556316

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41556316(A;A)
Make rs41556316(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271329
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41556316
ebirs41556316
HLIrs41556316
Exacrs41556316
Varsomers41556316
Maprs41556316
PheGenIrs41556316
hapmaprs41556316
1000 genomesrs41556316
hgdprs41556316
ensemblrs41556316
gopubmedrs41556316
geneviewrs41556316
scholarrs41556316
googlers41556316
pharmgkbrs41556316
gwascentralrs41556316
openSNPrs41556316
23andMers41556316
23andMe allrs41556316
SNP Nexus

SNPshotrs41556316
SNPdbers41556316
MSV3drs41556316
GWAS Ctlgrs41556316
Max Magnitude0
ClinVar
Risk rs41556316(A,C,T;A,C,T)
Alt rs41556316(A,C,T;A,C,T)
Reference rs41556316(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239106C>A; NC_000006.11:g.31239106C>G; NC_000006.11:g.31239106C>T
CLNSRC
CLNACC