Rs104894851

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Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894851(A;A)
Make rs104894851(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101398920
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs104894851
PheGenIrs104894851
nextbiors104894851
hapmaprs104894851
1000 genomesrs104894851
hgdprs104894851
ensemblrs104894851
gopubmedrs104894851
geneviewrs104894851
scholarrs104894851
googlers104894851
pharmgkbrs104894851
gwascentralrs104894851
openSNPrs104894851
23andMers104894851
23andMe allrs104894851
SNP Nexus

SNPshotrs104894851
SNPdbers104894851
MSV3drs104894851
Max Magnitude0
OMIM300644
Desc
Variant0058
Relatedalso
ClinVar
Risk rs104894851(A;A)
Alt rs104894851(A;A)
Reference rs104894851(C;C)
Significance Pathogenic
Disease Fabry's disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry's disease
Reversed 1
HGVS NC_000023.10:g.100653908G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011517.4,