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rs786205204

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205204(A;A)
Make rs786205204(A;G)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154366731
GeneFLNA
is asnp
is mentioned by
dbSNPrs786205204
ebirs786205204
HLIrs786205204
Exacrs786205204
Varsomers786205204
Maprs786205204
PheGenIrs786205204
hapmaprs786205204
1000 genomesrs786205204
hgdprs786205204
ensemblrs786205204
gopubmedrs786205204
geneviewrs786205204
scholarrs786205204
googlers786205204
pharmgkbrs786205204
gwascentralrs786205204
openSNPrs786205204
23andMers786205204
23andMe allrs786205204
SNP Nexus

SNPshotrs786205204
SNPdbers786205204
MSV3drs786205204
GWAS Ctlgrs786205204
Max Magnitude0
ClinVar
Risk rs786205204(A;A)
Alt rs786205204(A;A)
Reference rs786205204(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.153595099C>T
CLNSRC
CLNACC RCV000170426.1,