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rs786205002

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786205002(-;-)
Make rs786205002(-;C)
Make rs786205002(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767535
GeneFOXG1
is asnp
is mentioned by
dbSNPrs786205002
ebirs786205002
HLIrs786205002
Exacrs786205002
Varsomers786205002
Maprs786205002
PheGenIrs786205002
hapmaprs786205002
1000 genomesrs786205002
hgdprs786205002
ensemblrs786205002
gopubmedrs786205002
geneviewrs786205002
scholarrs786205002
googlers786205002
pharmgkbrs786205002
gwascentralrs786205002
openSNPrs786205002
23andMers786205002
23andMe allrs786205002
SNP Nexus

SNPshotrs786205002
SNPdbers786205002
MSV3drs786205002
GWAS Ctlgrs786205002
Max Magnitude0
ClinVar
Risk rs786205002(C;C)
Alt rs786205002(C;C)
Reference rs786205002(;)
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.29236741dupC
CLNSRC
CLNACC RCV000170074.1, RCV000187488.1,