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rs41544614

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41544614(C;C)
Make rs41544614(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271024
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41544614
ebirs41544614
HLIrs41544614
Exacrs41544614
Varsomers41544614
Maprs41544614
PheGenIrs41544614
hapmaprs41544614
1000 genomesrs41544614
hgdprs41544614
ensemblrs41544614
gopubmedrs41544614
geneviewrs41544614
scholarrs41544614
googlers41544614
pharmgkbrs41544614
gwascentralrs41544614
openSNPrs41544614
23andMers41544614
23andMe allrs41544614
SNP Nexus

SNPshotrs41544614
SNPdbers41544614
MSV3drs41544614
GWAS Ctlgrs41544614
GMAF0.06566
Max Magnitude0
ClinVar
Risk rs41544614(C;C)
Alt rs41544614(C;C)
Reference rs41544614(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238801C>G
CLNSRC
CLNACC