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rs41553316

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41553316(C;T)
Make rs41553316(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271218
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41553316
ebirs41553316
HLIrs41553316
Exacrs41553316
Varsomers41553316
Maprs41553316
PheGenIrs41553316
hapmaprs41553316
1000 genomesrs41553316
hgdprs41553316
ensemblrs41553316
gopubmedrs41553316
geneviewrs41553316
scholarrs41553316
googlers41553316
pharmgkbrs41553316
gwascentralrs41553316
openSNPrs41553316
23andMers41553316
23andMe allrs41553316
SNP Nexus

SNPshotrs41553316
SNPdbers41553316
MSV3drs41553316
GWAS Ctlgrs41553316
Max Magnitude0
ClinVar
Risk rs41553316(A,T;A,T)
Alt rs41553316(A,T;A,T)
Reference rs41553316(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238995G>A; NC_000006.11:g.31238995G>T
CLNSRC
CLNACC