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rs41561720

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41561720(A;A)
Make rs41561720(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271142
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41561720
ebirs41561720
HLIrs41561720
Exacrs41561720
Varsomers41561720
Maprs41561720
PheGenIrs41561720
hapmaprs41561720
1000 genomesrs41561720
hgdprs41561720
ensemblrs41561720
gopubmedrs41561720
geneviewrs41561720
scholarrs41561720
googlers41561720
pharmgkbrs41561720
gwascentralrs41561720
openSNPrs41561720
23andMers41561720
23andMe allrs41561720
SNP Nexus

SNPshotrs41561720
SNPdbers41561720
MSV3drs41561720
GWAS Ctlgrs41561720
Max Magnitude0
ClinVar
Risk rs41561720(A,T;A,T)
Alt rs41561720(A,T;A,T)
Reference rs41561720(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238919G>A; NC_000006.11:g.31238919G>T
CLNSRC
CLNACC