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rs28935196

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs28935196(C;C)
Make rs28935196(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101401695
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs28935196
ebirs28935196
HLIrs28935196
Exacrs28935196
Varsomers28935196
Maprs28935196
PheGenIrs28935196
hapmaprs28935196
1000 genomesrs28935196
hgdprs28935196
ensemblrs28935196
gopubmedrs28935196
geneviewrs28935196
scholarrs28935196
googlers28935196
pharmgkbrs28935196
gwascentralrs28935196
openSNPrs28935196
23andMers28935196
23andMe allrs28935196
SNP Nexus

SNPshotrs28935196
SNPdbers28935196
MSV3drs28935196
GWAS Ctlgrs28935196
Max Magnitude0
OMIM300644
Desc
Variant0016
Relatedalso
ClinVar
Risk rs28935196(C;C)
Alt rs28935196(C;C)
Reference rs28935196(T;T)
Significance Pathogenic
Disease Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease
Reversed 1
HGVS NC_000023.10:g.100656683A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000011475.2,