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rs730880443

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880443(G;T)
Make rs730880443(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position101403945
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs730880443
ebirs730880443
HLIrs730880443
Exacrs730880443
Varsomers730880443
Maprs730880443
PheGenIrs730880443
hapmaprs730880443
1000 genomesrs730880443
hgdprs730880443
ensemblrs730880443
gopubmedrs730880443
geneviewrs730880443
scholarrs730880443
googlers730880443
pharmgkbrs730880443
gwascentralrs730880443
openSNPrs730880443
23andMers730880443
23andMe allrs730880443
SNP Nexus

SNPshotrs730880443
SNPdbers730880443
MSV3drs730880443
GWAS Ctlgrs730880443
Max Magnitude0
ClinVar
Risk rs730880443(T;T)
Alt rs730880443(T;T)
Reference rs730880443(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.100658933C>A
CLNSRC
CLNACC RCV000157885.1,