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rs786205177

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205177(G;T)
Make rs786205177(T;T)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154365487
GeneFLNA
is asnp
is mentioned by
dbSNPrs786205177
ebirs786205177
HLIrs786205177
Exacrs786205177
Varsomers786205177
Maprs786205177
PheGenIrs786205177
hapmaprs786205177
1000 genomesrs786205177
hgdprs786205177
ensemblrs786205177
gopubmedrs786205177
geneviewrs786205177
scholarrs786205177
googlers786205177
pharmgkbrs786205177
gwascentralrs786205177
openSNPrs786205177
23andMers786205177
23andMe allrs786205177
SNP Nexus

SNPshotrs786205177
SNPdbers786205177
MSV3drs786205177
GWAS Ctlgrs786205177
Max Magnitude0
ClinVar
Risk rs786205177(T;T)
Alt rs786205177(T;T)
Reference rs786205177(G;G)
Significance Pathogenic
Disease X-linked periventricular heterotopia
Variation info
Gene FLNA
CLNDBN X-linked periventricular heterotopia
Reversed 1
HGVS NC_000023.10:g.153593855C>A
CLNSRC
CLNACC RCV000170397.1,