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rs398122812

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122812(A;A)
Make rs398122812(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154348897
GeneFLNA
is asnp
is mentioned by
dbSNPrs398122812
ebirs398122812
HLIrs398122812
Exacrs398122812
Varsomers398122812
Maprs398122812
PheGenIrs398122812
hapmaprs398122812
1000 genomesrs398122812
hgdprs398122812
ensemblrs398122812
gopubmedrs398122812
geneviewrs398122812
scholarrs398122812
googlers398122812
pharmgkbrs398122812
gwascentralrs398122812
openSNPrs398122812
23andMers398122812
23andMe allrs398122812
SNP Nexus

SNPshotrs398122812
SNPdbers398122812
MSV3drs398122812
GWAS Ctlgrs398122812
Max Magnitude0
ClinVar
Risk rs398122812(A;A)
Alt rs398122812(A;A)
Reference rs398122812(G;G)
Significance Pathogenic
Disease X-linked periventricular heterotopia
Variation info
Gene FLNA
CLNDBN X-linked periventricular heterotopia
Reversed 1
HGVS NC_000023.10:g.153577265C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000022819.17,