Rs104894838

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Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894838(G;G)
Make rs104894838(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101400699
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs104894838
Exacrs104894838
PheGenIrs104894838
nextbiors104894838
hapmaprs104894838
1000 genomesrs104894838
hgdprs104894838
ensemblrs104894838
gopubmedrs104894838
geneviewrs104894838
scholarrs104894838
googlers104894838
pharmgkbrs104894838
gwascentralrs104894838
openSNPrs104894838
23andMers104894838
23andMe allrs104894838
SNP Nexus

SNPshotrs104894838
SNPdbers104894838
MSV3drs104894838
OMIM300644
Desc
Variant0017
Relatedalso
ClinVar
Risk rs104894838(G;G)
Alt rs104894838(G;G)
Reference rs104894838(T;T)
Significance Pathogenic
Disease Fabry's disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry's disease
Reversed 1
HGVS NC_000023.10:g.100655687A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011476.3,