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rs786205007

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205007(A;A)
Make rs786205007(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767968
GeneFOXG1
is asnp
is mentioned by
dbSNPrs786205007
ebirs786205007
HLIrs786205007
Exacrs786205007
Varsomers786205007
Maprs786205007
PheGenIrs786205007
hapmaprs786205007
1000 genomesrs786205007
hgdprs786205007
ensemblrs786205007
gopubmedrs786205007
geneviewrs786205007
scholarrs786205007
googlers786205007
pharmgkbrs786205007
gwascentralrs786205007
openSNPrs786205007
23andMers786205007
23andMe allrs786205007
SNP Nexus

SNPshotrs786205007
SNPdbers786205007
MSV3drs786205007
GWAS Ctlgrs786205007
Max Magnitude0
ClinVar
Risk rs786205007(A;A)
Alt rs786205007(A;A)
Reference rs786205007(G;G)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene FOXG1
CLNDBN Rett syndrome, congenital variant
Reversed 0
HGVS NC_000014.8:g.29237174G>A
CLNSRC
CLNACC RCV000170080.1,