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rs730880441

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880441(C;T)
Make rs730880441(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position101398014
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs730880441
ebirs730880441
HLIrs730880441
Exacrs730880441
Varsomers730880441
Maprs730880441
PheGenIrs730880441
hapmaprs730880441
1000 genomesrs730880441
hgdprs730880441
ensemblrs730880441
gopubmedrs730880441
geneviewrs730880441
scholarrs730880441
googlers730880441
pharmgkbrs730880441
gwascentralrs730880441
openSNPrs730880441
23andMers730880441
23andMe allrs730880441
SNP Nexus

SNPshotrs730880441
SNPdbers730880441
MSV3drs730880441
GWAS Ctlgrs730880441
Max Magnitude0
ClinVar
Risk rs730880441(T;T)
Alt rs730880441(T;T)
Reference rs730880441(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.100653002G>A
CLNSRC
CLNACC RCV000157883.2,