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rs41563216

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41563216(C;T)
Make rs41563216(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271320
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41563216
ebirs41563216
HLIrs41563216
Exacrs41563216
Varsomers41563216
Maprs41563216
PheGenIrs41563216
hapmaprs41563216
1000 genomesrs41563216
hgdprs41563216
ensemblrs41563216
gopubmedrs41563216
geneviewrs41563216
scholarrs41563216
googlers41563216
pharmgkbrs41563216
gwascentralrs41563216
openSNPrs41563216
23andMers41563216
23andMe allrs41563216
SNP Nexus

SNPshotrs41563216
SNPdbers41563216
MSV3drs41563216
GWAS Ctlgrs41563216
Max Magnitude0
ClinVar
Risk rs41563216(T;T)
Alt rs41563216(T;T)
Reference rs41563216(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239097G>A
CLNSRC
CLNACC