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rs786205009

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205009(C;T)
Make rs786205009(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28768009
GeneFOXG1
is asnp
is mentioned by
dbSNPrs786205009
ebirs786205009
HLIrs786205009
Exacrs786205009
Varsomers786205009
Maprs786205009
PheGenIrs786205009
hapmaprs786205009
1000 genomesrs786205009
hgdprs786205009
ensemblrs786205009
gopubmedrs786205009
geneviewrs786205009
scholarrs786205009
googlers786205009
pharmgkbrs786205009
gwascentralrs786205009
openSNPrs786205009
23andMers786205009
23andMe allrs786205009
SNP Nexus

SNPshotrs786205009
SNPdbers786205009
MSV3drs786205009
GWAS Ctlgrs786205009
Max Magnitude0
ClinVar
Risk rs786205009(T;T)
Alt rs786205009(T;T)
Reference rs786205009(C;C)
Significance Pathogenic
Disease Rett syndrome not provided
Variation info
Gene FOXG1
CLNDBN Rett syndrome, congenital variant not provided
Reversed 0
HGVS NC_000014.8:g.29237215C>T
CLNSRC
CLNACC RCV000170082.1, RCV000187465.1,