Have questions? Visit https://www.reddit.com/r/SNPedia

rs786200973

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786200973(-;-)
Make rs786200973(-;AA)
Make rs786200973(AA;AA)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154357600
GeneFLNA
is asnp
is mentioned by
dbSNPrs786200973
ebirs786200973
HLIrs786200973
Exacrs786200973
Varsomers786200973
Maprs786200973
PheGenIrs786200973
hapmaprs786200973
1000 genomesrs786200973
hgdprs786200973
ensemblrs786200973
gopubmedrs786200973
geneviewrs786200973
scholarrs786200973
googlers786200973
pharmgkbrs786200973
gwascentralrs786200973
openSNPrs786200973
23andMers786200973
23andMe allrs786200973
SNP Nexus

SNPshotrs786200973
SNPdbers786200973
MSV3drs786200973
GWAS Ctlgrs786200973
Max Magnitude0
ClinVar
Risk rs786200973(AA;AA)
Alt rs786200973(AA;AA)
Reference rs786200973(;)
Significance Pathogenic
Disease not provided Oto-palato-digital syndrome X-linked periventricular heterotopia
Variation info
Gene FLNA
CLNDBN not provided Oto-palato-digital syndrome, type I X-linked periventricular heterotopia
Reversed 1
HGVS NC_000023.10:g.153585969_153585970dupTT
CLNSRC
CLNACC RCV000153252.2, RCV000176923.1, RCV000176924.1,