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rs150547672

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs150547672(A;G)
Make rs150547672(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101407896
GeneGLA, HNRNPH2, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs150547672
ebirs150547672
HLIrs150547672
Exacrs150547672
Varsomers150547672
Maprs150547672
PheGenIrs150547672
hapmaprs150547672
1000 genomesrs150547672
hgdprs150547672
ensemblrs150547672
gopubmedrs150547672
geneviewrs150547672
scholarrs150547672
googlers150547672
pharmgkbrs150547672
gwascentralrs150547672
openSNPrs150547672
23andMers150547672
23andMe allrs150547672
SNP Nexus

SNPshotrs150547672
SNPdbers150547672
MSV3drs150547672
GWAS Ctlgrs150547672
Max Magnitude0
ClinVar
Risk rs150547672(G;G)
Alt rs150547672(G;G)
Reference rs150547672(A;A)
Significance Drug-response
Disease not specified not provided Deoxygalactonojirimycin response Fabry disease
Variation info
Gene HNRNPH2 RPL36A-HNRNPH2 GLA
CLNDBN not specified not provided Deoxygalactonojirimycin response Fabry disease
Reversed 0
HGVS NC_000023.10:g.100662884A>G
CLNSRC
CLNACC RCV000035313.3, RCV000157875.1, RCV000209183.1, RCV000209748.2,