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rs730880449

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880449(A;A)
Make rs730880449(A;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position101400684
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs730880449
ebirs730880449
HLIrs730880449
Exacrs730880449
Varsomers730880449
Maprs730880449
PheGenIrs730880449
hapmaprs730880449
1000 genomesrs730880449
hgdprs730880449
ensemblrs730880449
gopubmedrs730880449
geneviewrs730880449
scholarrs730880449
googlers730880449
pharmgkbrs730880449
gwascentralrs730880449
openSNPrs730880449
23andMers730880449
23andMe allrs730880449
SNP Nexus

SNPshotrs730880449
SNPdbers730880449
MSV3drs730880449
GWAS Ctlgrs730880449
Max Magnitude0
ClinVar
Risk rs730880449(A;A)
Alt rs730880449(A;A)
Reference rs730880449(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.100655672A>T
CLNSRC
CLNACC RCV000157895.1,