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rs398123621

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs398123621(AA;AA)
Make rs398123621(AA;TC)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154354909
GeneFLNA
is asnp
is mentioned by
dbSNPrs398123621
ebirs398123621
HLIrs398123621
Exacrs398123621
Varsomers398123621
Maprs398123621
PheGenIrs398123621
hapmaprs398123621
1000 genomesrs398123621
hgdprs398123621
ensemblrs398123621
gopubmedrs398123621
geneviewrs398123621
scholarrs398123621
googlers398123621
pharmgkbrs398123621
gwascentralrs398123621
openSNPrs398123621
23andMers398123621
23andMe allrs398123621
SNP Nexus

SNPshotrs398123621
SNPdbers398123621
MSV3drs398123621
GWAS Ctlgrs398123621
Max Magnitude0
ClinVar
Risk rs398123621(AA;AA)
Alt rs398123621(AA;AA)
Reference rs398123621(TC;TC)
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.153583277_153583278delGAinsTT
CLNSRC ClinVar
CLNACC RCV000079701.3, RCV000177454.1, RCV000177455.1,