Rs104894836

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Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894836(G;G)
Make rs104894836(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101407738
GeneGLA, HNRNPH2
is asnp
is mentioned by
dbSNPrs104894836
Exacrs104894836
PheGenIrs104894836
nextbiors104894836
hapmaprs104894836
1000 genomesrs104894836
hgdprs104894836
ensemblrs104894836
gopubmedrs104894836
geneviewrs104894836
scholarrs104894836
googlers104894836
pharmgkbrs104894836
gwascentralrs104894836
openSNPrs104894836
23andMers104894836
23andMe allrs104894836
SNP Nexus

SNPshotrs104894836
SNPdbers104894836
MSV3drs104894836
Max Magnitude0
OMIM300644
Desc
Variant0013
Relatedalso
ClinVar
Risk rs104894836(G;G)
Alt rs104894836(G;G)
Reference rs104894836(T;T)
Significance Pathogenic
Disease Fabry's disease
Variation info
Gene RPL36A-HNRNPH2 HNRNPH2 GLA
CLNDBN Fabry's disease
Reversed 1
HGVS NC_000023.10:g.100662726A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011472.3,