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rs863223295

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223295(C;C)
Make rs863223295(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154367639
GeneFLNA
is asnp
is mentioned by
dbSNPrs863223295
ebirs863223295
HLIrs863223295
Exacrs863223295
Varsomers863223295
Maprs863223295
PheGenIrs863223295
hapmaprs863223295
1000 genomesrs863223295
hgdprs863223295
ensemblrs863223295
gopubmedrs863223295
geneviewrs863223295
scholarrs863223295
googlers863223295
pharmgkbrs863223295
gwascentralrs863223295
openSNPrs863223295
23andMers863223295
23andMe allrs863223295
SNP Nexus

SNPshotrs863223295
SNPdbers863223295
MSV3drs863223295
GWAS Ctlgrs863223295
Max Magnitude0
ClinVar
Risk rs863223295(C;C)
Alt rs863223295(C;C)
Reference rs863223295(T;T)
Significance Pathogenic
Disease X-linked periventricular heterotopia
Variation info
Gene FLNA
CLNDBN X-linked periventricular heterotopia
Reversed 1
HGVS NC_000023.10:g.153596007A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000012514.22,