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rs2975057

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2975057(C;T)
Make rs2975057(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29945394
GeneHLA-A
is asnp
is mentioned by
dbSNPrs2975057
ebirs2975057
HLIrs2975057
Exacrs2975057
Varsomers2975057
Maprs2975057
PheGenIrs2975057
hapmaprs2975057
1000 genomesrs2975057
hgdprs2975057
ensemblrs2975057
gopubmedrs2975057
geneviewrs2975057
scholarrs2975057
googlers2975057
pharmgkbrs2975057
gwascentralrs2975057
openSNPrs2975057
23andMers2975057
23andMe allrs2975057
SNP Nexus

SNPshotrs2975057
SNPdbers2975057
MSV3drs2975057
GWAS Ctlgrs2975057
GMAF0.3168
Max Magnitude0
ClinVar
Risk rs2975057(T;T)
Alt rs2975057(T;T)
Reference rs2975057(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 1
HGVS NC_000006.11:g.29913171G>A
CLNSRC
CLNACC