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rs863223299

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223299(-;-)
Make rs863223299(-;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154359402
GeneFLNA
is asnp
is mentioned by
dbSNPrs863223299
dbSNP (old)rs863223299
ClinGenrs863223299
ebirs863223299
HLIrs863223299
Exacrs863223299
Varsomers863223299
Maprs863223299
PheGenIrs863223299
Biobankrs863223299
1000 genomesrs863223299
hgdprs863223299
ensemblrs863223299
gopubmedrs863223299
geneviewrs863223299
scholarrs863223299
googlers863223299
pharmgkbrs863223299
gwascentralrs863223299
openSNPrs863223299
23andMers863223299
23andMe allrs863223299
SNP Nexus

SNPshotrs863223299
SNPdbers863223299
MSV3drs863223299
GWAS Ctlgrs863223299
Max Magnitude0
ClinVar
Risk rs863223299(-;-)
Alt rs863223299(-;-)
Reference Rs863223299(G;G)
Significance Pathogenic
Disease Periventricular nodular heterotopia 1
Variation info
Gene FLNA
CLNDBN Periventricular nodular heterotopia 1
Reversed 1
HGVS NC_000023.10:g.153587770delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000012530.15,