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rs78176797

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs78176797(C;C)
Make rs78176797(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270287
GeneHLA-C
is asnp
is mentioned by
dbSNPrs78176797
ebirs78176797
HLIrs78176797
Exacrs78176797
Varsomers78176797
Maprs78176797
PheGenIrs78176797
hapmaprs78176797
1000 genomesrs78176797
hgdprs78176797
ensemblrs78176797
gopubmedrs78176797
geneviewrs78176797
scholarrs78176797
googlers78176797
pharmgkbrs78176797
gwascentralrs78176797
openSNPrs78176797
23andMers78176797
23andMe allrs78176797
SNP Nexus

SNPshotrs78176797
SNPdbers78176797
MSV3drs78176797
GWAS Ctlgrs78176797
Max Magnitude0
ClinVar
Risk rs78176797(C;C)
Alt rs78176797(C;C)
Reference rs78176797(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238064A>G
CLNSRC
CLNACC