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rs730880452

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880452(C;T)
Make rs730880452(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position101398522
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs730880452
ebirs730880452
HLIrs730880452
Exacrs730880452
Varsomers730880452
Maprs730880452
PheGenIrs730880452
hapmaprs730880452
1000 genomesrs730880452
hgdprs730880452
ensemblrs730880452
gopubmedrs730880452
geneviewrs730880452
scholarrs730880452
googlers730880452
pharmgkbrs730880452
gwascentralrs730880452
openSNPrs730880452
23andMers730880452
23andMe allrs730880452
SNP Nexus

SNPshotrs730880452
SNPdbers730880452
MSV3drs730880452
GWAS Ctlgrs730880452
Max Magnitude0
ClinVar
Risk rs730880452(T;T)
Alt rs730880452(T;T)
Reference rs730880452(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.100653510G>A
CLNSRC
CLNACC RCV000157902.1,