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rs76638752

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs76638752(C;T)
Make rs76638752(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271662
GeneHLA-C
is asnp
is mentioned by
dbSNPrs76638752
ebirs76638752
HLIrs76638752
Exacrs76638752
Varsomers76638752
Maprs76638752
PheGenIrs76638752
hapmaprs76638752
1000 genomesrs76638752
hgdprs76638752
ensemblrs76638752
gopubmedrs76638752
geneviewrs76638752
scholarrs76638752
googlers76638752
pharmgkbrs76638752
gwascentralrs76638752
openSNPrs76638752
23andMers76638752
23andMe allrs76638752
SNP Nexus

SNPshotrs76638752
SNPdbers76638752
MSV3drs76638752
GWAS Ctlgrs76638752
Max Magnitude0
ClinVar
Risk rs76638752(T;T)
Alt rs76638752(T;T)
Reference rs76638752(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239439G>A
CLNSRC
CLNACC