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rs786205181

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205181(-;-)
Make rs786205181(-;A)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154371109
GeneFLNA
is asnp
is mentioned by
dbSNPrs786205181
ebirs786205181
HLIrs786205181
Exacrs786205181
Varsomers786205181
Maprs786205181
PheGenIrs786205181
hapmaprs786205181
1000 genomesrs786205181
hgdprs786205181
ensemblrs786205181
gopubmedrs786205181
geneviewrs786205181
scholarrs786205181
googlers786205181
pharmgkbrs786205181
gwascentralrs786205181
openSNPrs786205181
23andMers786205181
23andMe allrs786205181
SNP Nexus

SNPshotrs786205181
SNPdbers786205181
MSV3drs786205181
GWAS Ctlgrs786205181
Max Magnitude0
ClinVar
Risk rs786205181(;)
Alt rs786205181(;)
Reference rs786205181(A;A)
Significance Probable-Pathogenic
Disease X-linked periventricular heterotopia
Variation info
Gene FLNA
CLNDBN X-linked periventricular heterotopia
Reversed 1
HGVS NC_000023.10:g.153599477delT
CLNSRC Claritas Genomics
CLNACC RCV000170401.1,