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rs786205199

From SNPedia

Orientationminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs786205199(-;-)
Make rs786205199(-;TG)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154355020
GeneFLNA
is asnp
is mentioned by
dbSNPrs786205199
ebirs786205199
HLIrs786205199
Exacrs786205199
Varsomers786205199
Maprs786205199
PheGenIrs786205199
hapmaprs786205199
1000 genomesrs786205199
hgdprs786205199
ensemblrs786205199
gopubmedrs786205199
geneviewrs786205199
scholarrs786205199
googlers786205199
pharmgkbrs786205199
gwascentralrs786205199
openSNPrs786205199
23andMers786205199
23andMe allrs786205199
SNP Nexus

SNPshotrs786205199
SNPdbers786205199
MSV3drs786205199
GWAS Ctlgrs786205199
Max Magnitude0
ClinVar
Risk rs786205199(;)
Alt rs786205199(;)
Reference rs786205199(TG;TG)
Significance Probable-Pathogenic
Disease X-linked periventricular heterotopia
Variation info
Gene FLNA
CLNDBN X-linked periventricular heterotopia
Reversed 1
HGVS NC_000023.10:g.153583388_153583389delCA
CLNSRC
CLNACC RCV000170421.1,