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rs41563421

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41563421(A;A)
Make rs41563421(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271296
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41563421
ebirs41563421
HLIrs41563421
Exacrs41563421
Varsomers41563421
Maprs41563421
PheGenIrs41563421
hapmaprs41563421
1000 genomesrs41563421
hgdprs41563421
ensemblrs41563421
gopubmedrs41563421
geneviewrs41563421
scholarrs41563421
googlers41563421
pharmgkbrs41563421
gwascentralrs41563421
openSNPrs41563421
23andMers41563421
23andMe allrs41563421
SNP Nexus

SNPshotrs41563421
SNPdbers41563421
MSV3drs41563421
GWAS Ctlgrs41563421
Max Magnitude0
ClinVar
Risk rs41563421(A,T;A,T)
Alt rs41563421(A,T;A,T)
Reference rs41563421(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239073G>A; NC_000006.11:g.31239073G>T
CLNSRC
CLNACC