Rs104894852

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Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104894852(A;G)
Make rs104894852(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101397871
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs104894852
PheGenIrs104894852
nextbiors104894852
hapmaprs104894852
1000 genomesrs104894852
hgdprs104894852
ensemblrs104894852
gopubmedrs104894852
geneviewrs104894852
scholarrs104894852
googlers104894852
pharmgkbrs104894852
gwascentralrs104894852
openSNPrs104894852
23andMers104894852
23andMe allrs104894852
SNP Nexus

SNPshotrs104894852
SNPdbers104894852
MSV3drs104894852
Max Magnitude0
OMIM300644
Desc
Variant0059
Relatedalso
ClinVar
Risk rs104894852(G;G)
Alt rs104894852(G;G)
Reference rs104894852(A;A)
Significance Pathogenic
Disease Fabry's disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry's disease
Reversed 1
HGVS NC_000023.10:g.100652859T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011518.6,