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rs1611623

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1611623(A;A)
Make rs1611623(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355340
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1611623
ebirs1611623
HLIrs1611623
Exacrs1611623
Varsomers1611623
Maprs1611623
PheGenIrs1611623
hapmaprs1611623
1000 genomesrs1611623
hgdprs1611623
ensemblrs1611623
gopubmedrs1611623
geneviewrs1611623
scholarrs1611623
googlers1611623
pharmgkbrs1611623
gwascentralrs1611623
openSNPrs1611623
23andMers1611623
23andMe allrs1611623
SNP Nexus

SNPshotrs1611623
SNPdbers1611623
MSV3drs1611623
GWAS Ctlgrs1611623
Max Magnitude0
ClinVar
Risk rs1611623(A,G,T;A,G,T)
Alt rs1611623(A,G,T;A,G,T)
Reference rs1611623(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323117G>A; NC_000006.11:g.31323117G>C; NC_000006.11:g.31323117G>T
CLNSRC
CLNACC