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rs75991672

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs75991672(A;T)
Make rs75991672(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942919
GeneHLA-A
is asnp
is mentioned by
dbSNPrs75991672
ebirs75991672
HLIrs75991672
Exacrs75991672
Varsomers75991672
Maprs75991672
PheGenIrs75991672
hapmaprs75991672
1000 genomesrs75991672
hgdprs75991672
ensemblrs75991672
gopubmedrs75991672
geneviewrs75991672
scholarrs75991672
googlers75991672
pharmgkbrs75991672
gwascentralrs75991672
openSNPrs75991672
23andMers75991672
23andMe allrs75991672
SNP Nexus

SNPshotrs75991672
SNPdbers75991672
MSV3drs75991672
GWAS Ctlgrs75991672
Max Magnitude0
ClinVar
Risk rs75991672(T;T)
Alt rs75991672(T;T)
Reference rs75991672(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910696A>T
CLNSRC
CLNACC