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rs28935495

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs28935495(A;G)
Make rs28935495(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101398554
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs28935495
ebirs28935495
HLIrs28935495
Exacrs28935495
Varsomers28935495
Maprs28935495
PheGenIrs28935495
hapmaprs28935495
1000 genomesrs28935495
hgdprs28935495
ensemblrs28935495
gopubmedrs28935495
geneviewrs28935495
scholarrs28935495
googlers28935495
pharmgkbrs28935495
gwascentralrs28935495
openSNPrs28935495
23andMers28935495
23andMe allrs28935495
SNP Nexus

SNPshotrs28935495
SNPdbers28935495
MSV3drs28935495
GWAS Ctlgrs28935495
Max Magnitude0
OMIM300644
Desc
Variant0062
Relatedalso


ClinVar
Risk rs28935495(G;G)
Alt rs28935495(G;G)
Reference rs28935495(A;A)
Significance Pathogenic
Disease Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease
Reversed 1
HGVS NC_000023.10:g.100653542T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011521.2,