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rs77376497

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs77376497(C;C)
Make rs77376497(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271620
GeneHLA-C
is asnp
is mentioned by
dbSNPrs77376497
ebirs77376497
HLIrs77376497
Exacrs77376497
Varsomers77376497
Maprs77376497
PheGenIrs77376497
hapmaprs77376497
1000 genomesrs77376497
hgdprs77376497
ensemblrs77376497
gopubmedrs77376497
geneviewrs77376497
scholarrs77376497
googlers77376497
pharmgkbrs77376497
gwascentralrs77376497
openSNPrs77376497
23andMers77376497
23andMe allrs77376497
SNP Nexus

SNPshotrs77376497
SNPdbers77376497
MSV3drs77376497
GWAS Ctlgrs77376497
Max Magnitude0
ClinVar
Risk rs77376497(C;C)
Alt rs77376497(C;C)
Reference rs77376497(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239397A>G
CLNSRC
CLNACC