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rs41541318

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41541318(G;G)
Make rs41541318(G;T)
Make rs41541318(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269859
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41541318
ebirs41541318
HLIrs41541318
Exacrs41541318
Varsomers41541318
Maprs41541318
PheGenIrs41541318
hapmaprs41541318
1000 genomesrs41541318
hgdprs41541318
ensemblrs41541318
gopubmedrs41541318
geneviewrs41541318
scholarrs41541318
googlers41541318
pharmgkbrs41541318
gwascentralrs41541318
openSNPrs41541318
23andMers41541318
23andMe allrs41541318
SNP Nexus

SNPshotrs41541318
SNPdbers41541318
MSV3drs41541318
GWAS Ctlgrs41541318
GMAF0.01653
Max Magnitude0
ClinVar
Risk rs41541318(C,G,T;C,G,T)
Alt rs41541318(C,G,T;C,G,T)
Reference rs41541318(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237636T>C; NC_000006.11:g.31237636T>G
CLNSRC
CLNACC