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rs77244469

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs77244469(A;A)
Make rs77244469(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271301
GeneHLA-C
is asnp
is mentioned by
dbSNPrs77244469
ebirs77244469
HLIrs77244469
Exacrs77244469
Varsomers77244469
Maprs77244469
PheGenIrs77244469
hapmaprs77244469
1000 genomesrs77244469
hgdprs77244469
ensemblrs77244469
gopubmedrs77244469
geneviewrs77244469
scholarrs77244469
googlers77244469
pharmgkbrs77244469
gwascentralrs77244469
openSNPrs77244469
23andMers77244469
23andMe allrs77244469
SNP Nexus

SNPshotrs77244469
SNPdbers77244469
MSV3drs77244469
GWAS Ctlgrs77244469
Max Magnitude0
ClinVar
Risk rs77244469(A,C,T;A,C,T)
Alt rs77244469(A,C,T;A,C,T)
Reference rs77244469(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239078C>A; NC_000006.11:g.31239078C>G; NC_000006.11:g.31239078C>T
CLNSRC
CLNACC