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rs786205182

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205182(A;A)
Make rs786205182(A;T)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154364927
GeneFLNA
is asnp
is mentioned by
dbSNPrs786205182
ebirs786205182
HLIrs786205182
Exacrs786205182
Varsomers786205182
Maprs786205182
PheGenIrs786205182
hapmaprs786205182
1000 genomesrs786205182
hgdprs786205182
ensemblrs786205182
gopubmedrs786205182
geneviewrs786205182
scholarrs786205182
googlers786205182
pharmgkbrs786205182
gwascentralrs786205182
openSNPrs786205182
23andMers786205182
23andMe allrs786205182
SNP Nexus

SNPshotrs786205182
SNPdbers786205182
MSV3drs786205182
GWAS Ctlgrs786205182
Max Magnitude0
ClinVar
Risk rs786205182(A;A)
Alt rs786205182(A;A)
Reference rs786205182(T;T)
Significance Probable-Pathogenic
Disease X-linked periventricular heterotopia
Variation info
Gene FLNA
CLNDBN X-linked periventricular heterotopia
Reversed 1
HGVS NC_000023.10:g.153593295A>T
CLNSRC Claritas Genomics
CLNACC RCV000170403.1,