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rs786205188

From SNPedia

Orientationminus
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
ebirs786205188
HLIrs786205188
Exacrs786205188
Varsomers786205188
Maprs786205188
PheGenIrs786205188
hapmaprs786205188
1000 genomesrs786205188
hgdprs786205188
ensemblrs786205188
gopubmedrs786205188
geneviewrs786205188
scholarrs786205188
googlers786205188
pharmgkbrs786205188
gwascentralrs786205188
openSNPrs786205188
23andMers786205188
23andMe allrs786205188
SNP Nexus

SNPshotrs786205188
SNPdbers786205188
MSV3drs786205188
GWAS Ctlgrs786205188
Max Magnitude0
ClinVar
Risk rs786205188(;)
Alt rs786205188(;)
Reference rs786205188(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.153588634delC
CLNSRC
CLNACC RCV000170409.1,