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rs77659523

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs77659523(A;A)
Make rs77659523(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355563
GeneHLA-B
is asnp
is mentioned by
dbSNPrs77659523
ebirs77659523
HLIrs77659523
Exacrs77659523
Varsomers77659523
Maprs77659523
PheGenIrs77659523
hapmaprs77659523
1000 genomesrs77659523
hgdprs77659523
ensemblrs77659523
gopubmedrs77659523
geneviewrs77659523
scholarrs77659523
googlers77659523
pharmgkbrs77659523
gwascentralrs77659523
openSNPrs77659523
23andMers77659523
23andMe allrs77659523
SNP Nexus

SNPshotrs77659523
SNPdbers77659523
MSV3drs77659523
GWAS Ctlgrs77659523
Max Magnitude0
ClinVar
Risk rs77659523(A;A)
Alt rs77659523(A;A)
Reference rs77659523(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323340G>T
CLNSRC
CLNACC