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rs41540117

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41540117(C;C)
Make rs41540117(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270250
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41540117
ebirs41540117
HLIrs41540117
Exacrs41540117
Varsomers41540117
Maprs41540117
PheGenIrs41540117
hapmaprs41540117
1000 genomesrs41540117
hgdprs41540117
ensemblrs41540117
gopubmedrs41540117
geneviewrs41540117
scholarrs41540117
googlers41540117
pharmgkbrs41540117
gwascentralrs41540117
openSNPrs41540117
23andMers41540117
23andMe allrs41540117
SNP Nexus

SNPshotrs41540117
SNPdbers41540117
MSV3drs41540117
GWAS Ctlgrs41540117
GMAF0.1125
Max Magnitude0
ClinVar
Risk rs41540117(C,T;C,T)
Alt rs41540117(C,T;C,T)
Reference rs41540117(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238027C>A
CLNSRC
CLNACC