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rs77665001

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs77665001(A;A)
Make rs77665001(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355485
GeneHLA-B
is asnp
is mentioned by
dbSNPrs77665001
ebirs77665001
HLIrs77665001
Exacrs77665001
Varsomers77665001
Maprs77665001
PheGenIrs77665001
hapmaprs77665001
1000 genomesrs77665001
hgdprs77665001
ensemblrs77665001
gopubmedrs77665001
geneviewrs77665001
scholarrs77665001
googlers77665001
pharmgkbrs77665001
gwascentralrs77665001
openSNPrs77665001
23andMers77665001
23andMe allrs77665001
SNP Nexus

SNPshotrs77665001
SNPdbers77665001
MSV3drs77665001
GWAS Ctlgrs77665001
GMAF0.06107
Max Magnitude0
ClinVar
Risk rs77665001(A,C;A,C)
Alt rs77665001(A,C;A,C)
Reference rs77665001(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31323262G>C
CLNSRC
CLNACC