Rs104894840

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Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894840(A;A)
Make rs104894840(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101398906
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs104894840
PheGenIrs104894840
nextbiors104894840
hapmaprs104894840
1000 genomesrs104894840
hgdprs104894840
ensemblrs104894840
gopubmedrs104894840
geneviewrs104894840
scholarrs104894840
googlers104894840
pharmgkbrs104894840
gwascentralrs104894840
openSNPrs104894840
23andMers104894840
23andMe allrs104894840
SNP Nexus

SNPshotrs104894840
SNPdbers104894840
MSV3drs104894840
Max Magnitude0
OMIM300644
Desc
Variant0019
Relatedalso
ClinVar
Risk rs104894840(A;A)
Alt rs104894840(A;A)
Reference rs104894840(G;G)
Significance Pathogenic
Disease Fabry's disease not provided
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry's disease not provided
Reversed 1
HGVS NC_000023.10:g.100653894C>T
CLNSRC Emory University OMIM Allelic Variant
CLNACC RCV000011478.6, RCV000078294.1,