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rs786205201

From SNPedia

Orientationminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs786205201(-;-)
Make rs786205201(-;AA)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154352795
GeneFLNA
is asnp
is mentioned by
dbSNPrs786205201
ebirs786205201
HLIrs786205201
Exacrs786205201
Varsomers786205201
Maprs786205201
PheGenIrs786205201
hapmaprs786205201
1000 genomesrs786205201
hgdprs786205201
ensemblrs786205201
gopubmedrs786205201
geneviewrs786205201
scholarrs786205201
googlers786205201
pharmgkbrs786205201
gwascentralrs786205201
openSNPrs786205201
23andMers786205201
23andMe allrs786205201
SNP Nexus

SNPshotrs786205201
SNPdbers786205201
MSV3drs786205201
GWAS Ctlgrs786205201
Max Magnitude0
ClinVar
Risk rs786205201(;)
Alt rs786205201(;)
Reference rs786205201(AA;AA)
Significance Pathogenic
Disease X-linked periventricular heterotopia
Variation info
Gene FLNA
CLNDBN X-linked periventricular heterotopia
Reversed 1
HGVS NC_000023.10:g.153581163_153581164delTT
CLNSRC
CLNACC RCV000170423.1,