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rs730880439

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880439(C;G)
Make rs730880439(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position101398408
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs730880439
ebirs730880439
HLIrs730880439
Exacrs730880439
Varsomers730880439
Maprs730880439
PheGenIrs730880439
hapmaprs730880439
1000 genomesrs730880439
hgdprs730880439
ensemblrs730880439
gopubmedrs730880439
geneviewrs730880439
scholarrs730880439
googlers730880439
pharmgkbrs730880439
gwascentralrs730880439
openSNPrs730880439
23andMers730880439
23andMe allrs730880439
SNP Nexus

SNPshotrs730880439
SNPdbers730880439
MSV3drs730880439
GWAS Ctlgrs730880439
Max Magnitude0
ClinVar
Risk rs730880439(G;G)
Alt rs730880439(G;G)
Reference rs730880439(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.100653396G>C
CLNSRC
CLNACC RCV000157880.1,