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rs76907552

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs76907552(G;T)
Make rs76907552(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271229
GeneHLA-C
is asnp
is mentioned by
dbSNPrs76907552
ebirs76907552
HLIrs76907552
Exacrs76907552
Varsomers76907552
Maprs76907552
PheGenIrs76907552
hapmaprs76907552
1000 genomesrs76907552
hgdprs76907552
ensemblrs76907552
gopubmedrs76907552
geneviewrs76907552
scholarrs76907552
googlers76907552
pharmgkbrs76907552
gwascentralrs76907552
openSNPrs76907552
23andMers76907552
23andMe allrs76907552
SNP Nexus

SNPshotrs76907552
SNPdbers76907552
MSV3drs76907552
GWAS Ctlgrs76907552
GMAF0.2461
Max Magnitude0
ClinVar
Risk rs76907552(A,T;A,T)
Alt rs76907552(A,T;A,T)
Reference rs76907552(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31239006G>A; NC_000006.11:g.31239006G>T
CLNSRC
CLNACC