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rs730880447

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880447(A;A)
Make rs730880447(A;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position101400758
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs730880447
ebirs730880447
HLIrs730880447
Exacrs730880447
Varsomers730880447
Maprs730880447
PheGenIrs730880447
hapmaprs730880447
1000 genomesrs730880447
hgdprs730880447
ensemblrs730880447
gopubmedrs730880447
geneviewrs730880447
scholarrs730880447
googlers730880447
pharmgkbrs730880447
gwascentralrs730880447
openSNPrs730880447
23andMers730880447
23andMe allrs730880447
SNP Nexus

SNPshotrs730880447
SNPdbers730880447
MSV3drs730880447
GWAS Ctlgrs730880447
Max Magnitude0
ClinVar
Risk rs730880447(A;A)
Alt rs730880447(A;A)
Reference rs730880447(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.100655746C>T
CLNSRC
CLNACC RCV000157893.1,