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rs786205180

From SNPedia

Orientationminus
Geno Mag Summary
(ATAAG;ATAAG) 0 common in clinvar
Make rs786205180(-;-)
Make rs786205180(-;ATAAG)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154366562
GeneFLNA
is asnp
is mentioned by
dbSNPrs786205180
ebirs786205180
HLIrs786205180
Exacrs786205180
Varsomers786205180
Maprs786205180
PheGenIrs786205180
hapmaprs786205180
1000 genomesrs786205180
hgdprs786205180
ensemblrs786205180
gopubmedrs786205180
geneviewrs786205180
scholarrs786205180
googlers786205180
pharmgkbrs786205180
gwascentralrs786205180
openSNPrs786205180
23andMers786205180
23andMe allrs786205180
SNP Nexus

SNPshotrs786205180
SNPdbers786205180
MSV3drs786205180
GWAS Ctlgrs786205180
Max Magnitude0
ClinVar
Risk rs786205180(;)
Alt rs786205180(;)
Reference rs786205180(ATAAG;ATAAG)
Significance Probable-Pathogenic
Disease X-linked periventricular heterotopia
Variation info
Gene FLNA
CLNDBN X-linked periventricular heterotopia
Reversed 1
HGVS NC_000023.10:g.153594930_153594934delCTTAT
CLNSRC Claritas Genomics
CLNACC RCV000170400.1,