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rs730880455

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880455(C;C)
Make rs730880455(C;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position101407863
GeneGLA, HNRNPH2, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs730880455
ebirs730880455
HLIrs730880455
Exacrs730880455
Varsomers730880455
Maprs730880455
PheGenIrs730880455
hapmaprs730880455
1000 genomesrs730880455
hgdprs730880455
ensemblrs730880455
gopubmedrs730880455
geneviewrs730880455
scholarrs730880455
googlers730880455
pharmgkbrs730880455
gwascentralrs730880455
openSNPrs730880455
23andMers730880455
23andMe allrs730880455
SNP Nexus

SNPshotrs730880455
SNPdbers730880455
MSV3drs730880455
GWAS Ctlgrs730880455
Max Magnitude0
ClinVar
Risk rs730880455(C;C)
Alt rs730880455(C;C)
Reference rs730880455(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene HNRNPH2 RPL36A-HNRNPH2 GLA
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.100662851A>G
CLNSRC
CLNACC RCV000157906.1,