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rs41562714

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41562714(C;G)
Make rs41562714(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270761
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41562714
ebirs41562714
HLIrs41562714
Exacrs41562714
Varsomers41562714
Maprs41562714
PheGenIrs41562714
hapmaprs41562714
1000 genomesrs41562714
hgdprs41562714
ensemblrs41562714
gopubmedrs41562714
geneviewrs41562714
scholarrs41562714
googlers41562714
pharmgkbrs41562714
gwascentralrs41562714
openSNPrs41562714
23andMers41562714
23andMe allrs41562714
SNP Nexus

SNPshotrs41562714
SNPdbers41562714
MSV3drs41562714
GWAS Ctlgrs41562714
GMAF0.1391
Max Magnitude0
ClinVar
Risk rs41562714(G;G)
Alt rs41562714(G;G)
Reference rs41562714(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238538G>C
CLNSRC
CLNACC