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rs1632885

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1632885(A;C)
Make rs1632885(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944733
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1632885
ebirs1632885
HLIrs1632885
Exacrs1632885
Varsomers1632885
Maprs1632885
PheGenIrs1632885
hapmaprs1632885
1000 genomesrs1632885
hgdprs1632885
ensemblrs1632885
gopubmedrs1632885
geneviewrs1632885
scholarrs1632885
googlers1632885
pharmgkbrs1632885
gwascentralrs1632885
openSNPrs1632885
23andMers1632885
23andMe allrs1632885
SNP Nexus

SNPshotrs1632885
SNPdbers1632885
MSV3drs1632885
GWAS Ctlgrs1632885
GMAF0.3292
Max Magnitude0
ClinVar
Risk rs1632885(C;C)
Alt rs1632885(C;C)
Reference rs1632885(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 1
HGVS NC_000006.11:g.29912510T; NC_000006.11:g.29912510T>G
CLNSRC
CLNACC