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

rs28935485

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs28935485(C;G)
Make rs28935485(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101398534
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs28935485
ebirs28935485
HLIrs28935485
Exacrs28935485
Varsomers28935485
Maprs28935485
PheGenIrs28935485
hapmaprs28935485
1000 genomesrs28935485
hgdprs28935485
ensemblrs28935485
gopubmedrs28935485
geneviewrs28935485
scholarrs28935485
googlers28935485
pharmgkbrs28935485
gwascentralrs28935485
openSNPrs28935485
23andMers28935485
23andMe allrs28935485
SNP Nexus

SNPshotrs28935485
SNPdbers28935485
MSV3drs28935485
GWAS Ctlgrs28935485
Max Magnitude0
OMIM300644
Desc
Variant0008
Relatedalso


ClinVar
Risk rs28935485(G;G)
Alt rs28935485(G;G)
Reference rs28935485(C;C)
Significance Pathogenic
Disease Fabry disease not provided
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease, cardiac variant not provided
Reversed 1
HGVS NC_000023.10:g.100653522G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011468.5, RCV000157901.1,