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rs2975058

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2975058(C;T)
Make rs2975058(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944818
GeneHLA-A
is asnp
is mentioned by
dbSNPrs2975058
ebirs2975058
HLIrs2975058
Exacrs2975058
Varsomers2975058
Maprs2975058
PheGenIrs2975058
hapmaprs2975058
1000 genomesrs2975058
hgdprs2975058
ensemblrs2975058
gopubmedrs2975058
geneviewrs2975058
scholarrs2975058
googlers2975058
pharmgkbrs2975058
gwascentralrs2975058
openSNPrs2975058
23andMers2975058
23andMe allrs2975058
SNP Nexus

SNPshotrs2975058
SNPdbers2975058
MSV3drs2975058
GWAS Ctlgrs2975058
GMAF0.3127
Max Magnitude0
ClinVar
Risk rs2975058(T;T)
Alt rs2975058(T;T)
Reference rs2975058(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 1
HGVS NC_000006.11:g.29912595G>A
CLNSRC
CLNACC