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rs62687162

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs62687162(G;T)
Make rs62687162(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943543
GeneHLA-A
is asnp
is mentioned by
dbSNPrs62687162
ebirs62687162
HLIrs62687162
Exacrs62687162
Varsomers62687162
Maprs62687162
PheGenIrs62687162
hapmaprs62687162
1000 genomesrs62687162
hgdprs62687162
ensemblrs62687162
gopubmedrs62687162
geneviewrs62687162
scholarrs62687162
googlers62687162
pharmgkbrs62687162
gwascentralrs62687162
openSNPrs62687162
23andMers62687162
23andMe allrs62687162
SNP Nexus

SNPshotrs62687162
SNPdbers62687162
MSV3drs62687162
GWAS Ctlgrs62687162
Max Magnitude0
ClinVar
Risk rs62687162(A,C,T;A,C,T)
Alt rs62687162(A,C,T;A,C,T)
Reference rs62687162(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911320G>A; NC_000006.11:g.29911320G>C
CLNSRC
CLNACC