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rs1058372

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs1058372(C;C)
Make rs1058372(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position16148904
GeneEPHA2
is asnp
is mentioned by
dbSNPrs1058372
dbSNP (classic)rs1058372
ClinGenrs1058372
ebirs1058372
HLIrs1058372
Exacrs1058372
Gnomadrs1058372
Varsomers1058372
LitVarrs1058372
Maprs1058372
PheGenIrs1058372
Biobankrs1058372
1000 genomesrs1058372
hgdprs1058372
ensemblrs1058372
geneviewrs1058372
scholarrs1058372
googlers1058372
pharmgkbrs1058372
gwascentralrs1058372
openSNPrs1058372
23andMers1058372
SNPshotrs1058372
SNPdbers1058372
MSV3drs1058372
GWAS Ctlgrs1058372
Max Magnitude0
? (C;C) (C;G) (G;G) 28


[PMID 22829731OA-icon.png] Screening and structural evaluation of deleterious Non-Synonymous SNPs of ePHA2 gene involved in susceptibility to cataract formation