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rs786205178

From SNPedia

Orientationminus
Geno Mag Summary
(TCAG;TCAG) 0 common in clinvar
Make rs786205178(-;-)
Make rs786205178(-;TCAG)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154352312
GeneFLNA
is asnp
is mentioned by
dbSNPrs786205178
ebirs786205178
HLIrs786205178
Exacrs786205178
Varsomers786205178
Maprs786205178
PheGenIrs786205178
hapmaprs786205178
1000 genomesrs786205178
hgdprs786205178
ensemblrs786205178
gopubmedrs786205178
geneviewrs786205178
scholarrs786205178
googlers786205178
pharmgkbrs786205178
gwascentralrs786205178
openSNPrs786205178
23andMers786205178
23andMe allrs786205178
SNP Nexus

SNPshotrs786205178
SNPdbers786205178
MSV3drs786205178
GWAS Ctlgrs786205178
Max Magnitude0
ClinVar
Risk rs786205178(;)
Alt rs786205178(;)
Reference rs786205178(TCAG;TCAG)
Significance Pathogenic
Disease X-linked periventricular heterotopia not provided
Variation info
Gene FLNA
CLNDBN X-linked periventricular heterotopia not provided
Reversed 1
HGVS NC_000023.10:g.153580680_153580683delCTGA
CLNSRC
CLNACC RCV000170398.1, RCV000199583.1,