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rs786205188

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205188(-;-)
Make rs786205188(-;G)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154360266
GeneFLNA
is asnp
is mentioned by
dbSNPrs786205188
dbSNP (classic)rs786205188
ClinGenrs786205188
ebirs786205188
HLIrs786205188
Exacrs786205188
Gnomadrs786205188
Varsomers786205188
LitVarrs786205188
Maprs786205188
PheGenIrs786205188
Biobankrs786205188
1000 genomesrs786205188
hgdprs786205188
ensemblrs786205188
geneviewrs786205188
scholarrs786205188
googlers786205188
pharmgkbrs786205188
gwascentralrs786205188
openSNPrs786205188
23andMers786205188
SNPshotrs786205188
SNPdbers786205188
MSV3drs786205188
GWAS Ctlgrs786205188
Max Magnitude0
ClinVar
Risk rs786205188(-;-)
Alt rs786205188(-;-)
Reference Rs786205188(G;G)
Significance Probable-Pathogenic
Disease Periventricular nodular heterotopia 1
Variation info
Gene FLNA
CLNDBN Periventricular nodular heterotopia 1
Reversed 1
HGVS NC_000023.10:g.153588634delC
CLNSRC
CLNACC RCV000170409.1,