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rs28935197

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs28935197(A;G)
Make rs28935197(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101398942
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs28935197
ebirs28935197
HLIrs28935197
Exacrs28935197
Varsomers28935197
Maprs28935197
PheGenIrs28935197
hapmaprs28935197
1000 genomesrs28935197
hgdprs28935197
ensemblrs28935197
gopubmedrs28935197
geneviewrs28935197
scholarrs28935197
googlers28935197
pharmgkbrs28935197
gwascentralrs28935197
openSNPrs28935197
23andMers28935197
23andMe allrs28935197
SNP Nexus

SNPshotrs28935197
SNPdbers28935197
MSV3drs28935197
GWAS Ctlgrs28935197
Max Magnitude0
OMIM300644
Desc
Variant0018
Relatedalso
ClinVar
Risk rs28935197(G;G)
Alt rs28935197(G;G)
Reference rs28935197(A;A)
Significance Pathogenic
Disease Fabry disease not provided
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease not provided
Reversed 1
HGVS NC_000023.10:g.100653930T>C
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000011477.9, RCV000157896.3,