Rs104894829

From SNPedia
Jump to: navigation, search

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894829(A;A)
Make rs104894829(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101407773
GeneGLA, HNRNPH2
is asnp
is mentioned by
dbSNPrs104894829
Exacrs104894829
PheGenIrs104894829
nextbiors104894829
hapmaprs104894829
1000 genomesrs104894829
hgdprs104894829
ensemblrs104894829
gopubmedrs104894829
geneviewrs104894829
scholarrs104894829
googlers104894829
pharmgkbrs104894829
gwascentralrs104894829
openSNPrs104894829
23andMers104894829
23andMe allrs104894829
SNP Nexus

SNPshotrs104894829
SNPdbers104894829
MSV3drs104894829
OMIM300644
Desc
Variant0004
Relatedalso
ClinVar
Risk rs104894829(A;A)
Alt rs104894829(A;A)
Reference rs104894829(G;G)
Significance Pathogenic
Disease Fabry's disease
Variation info
Gene RPL36A-HNRNPH2 HNRNPH2 GLA
CLNDBN Fabry's disease
Reversed 1
HGVS NC_000023.10:g.100662761C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011463.4,