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rs41563115

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41563115(C;T)
Make rs41563115(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271116
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41563115
ebirs41563115
HLIrs41563115
Exacrs41563115
Varsomers41563115
Maprs41563115
PheGenIrs41563115
hapmaprs41563115
1000 genomesrs41563115
hgdprs41563115
ensemblrs41563115
gopubmedrs41563115
geneviewrs41563115
scholarrs41563115
googlers41563115
pharmgkbrs41563115
gwascentralrs41563115
openSNPrs41563115
23andMers41563115
23andMe allrs41563115
SNP Nexus

SNPshotrs41563115
SNPdbers41563115
MSV3drs41563115
GWAS Ctlgrs41563115
Max Magnitude0
ClinVar
Risk rs41563115(T;T)
Alt rs41563115(T;T)
Reference rs41563115(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238893G>A
CLNSRC
CLNACC