Have questions? Visit https://www.reddit.com/r/SNPedia

rs76778601

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs76778601(A;A)
Make rs76778601(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355324
GeneHLA-B
is asnp
is mentioned by
dbSNPrs76778601
ebirs76778601
HLIrs76778601
Exacrs76778601
Varsomers76778601
Maprs76778601
PheGenIrs76778601
hapmaprs76778601
1000 genomesrs76778601
hgdprs76778601
ensemblrs76778601
gopubmedrs76778601
geneviewrs76778601
scholarrs76778601
googlers76778601
pharmgkbrs76778601
gwascentralrs76778601
openSNPrs76778601
23andMers76778601
23andMe allrs76778601
SNP Nexus

SNPshotrs76778601
SNPdbers76778601
MSV3drs76778601
GWAS Ctlgrs76778601
Max Magnitude0
ClinVar
Risk rs76778601(A;A)
Alt rs76778601(A;A)
Reference rs76778601(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323101C>T
CLNSRC
CLNACC