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rs786204998

From SNPedia

Orientationplus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs786204998(CT;CT)
Make rs786204998(CT;TC)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767923
GeneFOXG1
is asnp
is mentioned by
dbSNPrs786204998
ebirs786204998
HLIrs786204998
Exacrs786204998
Varsomers786204998
Maprs786204998
PheGenIrs786204998
hapmaprs786204998
1000 genomesrs786204998
hgdprs786204998
ensemblrs786204998
gopubmedrs786204998
geneviewrs786204998
scholarrs786204998
googlers786204998
pharmgkbrs786204998
gwascentralrs786204998
openSNPrs786204998
23andMers786204998
23andMe allrs786204998
SNP Nexus

SNPshotrs786204998
SNPdbers786204998
MSV3drs786204998
GWAS Ctlgrs786204998
Max Magnitude0
ClinVar
Risk rs786204998(CT;CT)
Alt rs786204998(CT;CT)
Reference rs786204998(TC;TC)
Significance Pathogenic
Disease not provided Rett syndrome
Variation info
Gene FOXG1
CLNDBN not provided Rett syndrome, congenital variant
Reversed 0
HGVS NC_000014.8:g.29237129_29237130delTCinsCT
CLNSRC
CLNACC RCV000170068.1, RCV000194042.1,