Have questions? Visit https://www.reddit.com/r/SNPedia

rs28935486

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs28935486(A;T)
Make rs28935486(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101398795
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs28935486
ebirs28935486
HLIrs28935486
Exacrs28935486
Varsomers28935486
Maprs28935486
PheGenIrs28935486
hapmaprs28935486
1000 genomesrs28935486
hgdprs28935486
ensemblrs28935486
gopubmedrs28935486
geneviewrs28935486
scholarrs28935486
googlers28935486
pharmgkbrs28935486
gwascentralrs28935486
openSNPrs28935486
23andMers28935486
23andMe allrs28935486
SNP Nexus

SNPshotrs28935486
SNPdbers28935486
MSV3drs28935486
GWAS Ctlgrs28935486
Max Magnitude0
OMIM300644
Desc
Variant0021
Relatedalso


ClinVar
Risk rs28935486(T;T)
Alt rs28935486(T;T)
Reference rs28935486(A;A)
Significance Pathogenic
Disease Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease
Reversed 1
HGVS NC_000023.10:g.100653783T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011480.4,