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Rs104894839

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Orientationminus
is asnp
is mentioned by
dbSNPrs104894839
PheGenIrs104894839
hapmaprs104894839
1000 genomesrs104894839
hgdprs104894839
ensemblrs104894839
gopubmedrs104894839
geneviewrs104894839
scholarrs104894839
googlers104894839
pharmgkbrs104894839
gwascentralrs104894839
openSNPrs104894839
23andMers104894839
23andMe allrs104894839
SNP Nexus

SNPshotrs104894839
SNPdbers104894839
MSV3drs104894839
GeneGLA, RPL36A-HNRNPH2
ChromosomeX
Orientationminus
Position101398508
ReferenceGRCh38 38.1/141
Max Magnitude0
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894839(A;A)
Make rs104894839(A;G)
OMIM300644
Desc
Variant0024
Relatedalso
ClinVar
Risk rs104894839(A;A)
Alt rs104894839(A;A)
Reference rs104894839(G;G)
Significance 5
Disease Fabry's disease
ClinVar info, info
Gene RPL36A-HNRNPH2, GLA
CLNDBN Fabry's disease
Reversed 1
CLNHGVS NC_000023.10:g.100653496C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011483.3