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rs398123619

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123619(-;-)
Make rs398123619(-;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154371204
GeneFLNA
is asnp
is mentioned by
dbSNPrs398123619
ebirs398123619
HLIrs398123619
Exacrs398123619
Varsomers398123619
Maprs398123619
PheGenIrs398123619
hapmaprs398123619
1000 genomesrs398123619
hgdprs398123619
ensemblrs398123619
gopubmedrs398123619
geneviewrs398123619
scholarrs398123619
googlers398123619
pharmgkbrs398123619
gwascentralrs398123619
openSNPrs398123619
23andMers398123619
23andMe allrs398123619
SNP Nexus

SNPshotrs398123619
SNPdbers398123619
MSV3drs398123619
GWAS Ctlgrs398123619
Max Magnitude0
ClinVar
Risk rs398123619(;)
Alt rs398123619(;)
Reference rs398123619(C;C)
Significance Pathogenic
Disease not provided Oto-palato-digital syndrome X-linked periventricular heterotopia
Variation info
Gene FLNA
CLNDBN not provided Oto-palato-digital syndrome, type I X-linked periventricular heterotopia
Reversed 1
HGVS NC_000023.10:g.153599572delG
CLNSRC ClinVar
CLNACC RCV000079697.3, RCV000175695.1, RCV000175696.1,