Have questions? Visit https://www.reddit.com/r/SNPedia

rs863223296

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223296(A;A)
Make rs863223296(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154370872
GeneFLNA
is asnp
is mentioned by
dbSNPrs863223296
ebirs863223296
HLIrs863223296
Exacrs863223296
Varsomers863223296
Maprs863223296
PheGenIrs863223296
hapmaprs863223296
1000 genomesrs863223296
hgdprs863223296
ensemblrs863223296
gopubmedrs863223296
geneviewrs863223296
scholarrs863223296
googlers863223296
pharmgkbrs863223296
gwascentralrs863223296
openSNPrs863223296
23andMers863223296
23andMe allrs863223296
SNP Nexus

SNPshotrs863223296
SNPdbers863223296
MSV3drs863223296
GWAS Ctlgrs863223296
Max Magnitude0
ClinVar
Risk rs863223296(A;A)
Alt rs863223296(A;A)
Reference rs863223296(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.153599240C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012516.16,