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

rs786205202

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205202(G;T)
Make rs786205202(T;T)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154352370
GeneFLNA
is asnp
is mentioned by
dbSNPrs786205202
ebirs786205202
HLIrs786205202
Exacrs786205202
Varsomers786205202
Maprs786205202
PheGenIrs786205202
hapmaprs786205202
1000 genomesrs786205202
hgdprs786205202
ensemblrs786205202
gopubmedrs786205202
geneviewrs786205202
scholarrs786205202
googlers786205202
pharmgkbrs786205202
gwascentralrs786205202
openSNPrs786205202
23andMers786205202
23andMe allrs786205202
SNP Nexus

SNPshotrs786205202
SNPdbers786205202
MSV3drs786205202
GWAS Ctlgrs786205202
Max Magnitude0
ClinVar
Risk rs786205202(T;T)
Alt rs786205202(T;T)
Reference rs786205202(G;G)
Significance Probable-Pathogenic
Disease X-linked periventricular heterotopia
Variation info
Gene FLNA
CLNDBN X-linked periventricular heterotopia
Reversed 1
HGVS NC_000023.10:g.153580738C>A
CLNSRC
CLNACC RCV000170424.1,