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rs786205191

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205191(-;-)
Make rs786205191(-;G)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154359620
GeneFLNA
is asnp
is mentioned by
dbSNPrs786205191
ebirs786205191
HLIrs786205191
Exacrs786205191
Varsomers786205191
Maprs786205191
PheGenIrs786205191
hapmaprs786205191
1000 genomesrs786205191
hgdprs786205191
ensemblrs786205191
gopubmedrs786205191
geneviewrs786205191
scholarrs786205191
googlers786205191
pharmgkbrs786205191
gwascentralrs786205191
openSNPrs786205191
23andMers786205191
23andMe allrs786205191
SNP Nexus

SNPshotrs786205191
SNPdbers786205191
MSV3drs786205191
GWAS Ctlgrs786205191
Max Magnitude0
ClinVar
Risk rs786205191(;)
Alt rs786205191(;)
Reference rs786205191(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.153587988delC
CLNSRC Claritas Genomics
CLNACC RCV000170412.1,