Rs104894839

From SNPedia
Jump to: navigation, search

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894839(A;A)
Make rs104894839(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101398508
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs104894839
PheGenIrs104894839
nextbiors104894839
hapmaprs104894839
1000 genomesrs104894839
hgdprs104894839
ensemblrs104894839
gopubmedrs104894839
geneviewrs104894839
scholarrs104894839
googlers104894839
pharmgkbrs104894839
gwascentralrs104894839
openSNPrs104894839
23andMers104894839
23andMe allrs104894839
SNP Nexus

SNPshotrs104894839
SNPdbers104894839
MSV3drs104894839
Max Magnitude0
OMIM300644
Desc
Variant0024
Relatedalso
ClinVar
Risk rs104894839(A;A)
Alt rs104894839(A;A)
Reference rs104894839(G;G)
Significance Pathogenic
Disease Fabry's disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry's disease
Reversed 1
HGVS NC_000023.10:g.100653496C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011483.3,