Have questions? Visit https://www.reddit.com/r/SNPedia

rs786205000

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205000(C;T)
Make rs786205000(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767415
GeneFOXG1
is asnp
is mentioned by
dbSNPrs786205000
ebirs786205000
HLIrs786205000
Exacrs786205000
Varsomers786205000
Maprs786205000
PheGenIrs786205000
hapmaprs786205000
1000 genomesrs786205000
hgdprs786205000
ensemblrs786205000
gopubmedrs786205000
geneviewrs786205000
scholarrs786205000
googlers786205000
pharmgkbrs786205000
gwascentralrs786205000
openSNPrs786205000
23andMers786205000
23andMe allrs786205000
SNP Nexus

SNPshotrs786205000
SNPdbers786205000
MSV3drs786205000
GWAS Ctlgrs786205000
Max Magnitude0
ClinVar
Risk rs786205000(T;T)
Alt rs786205000(T;T)
Reference rs786205000(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29236621C>T
CLNSRC
CLNACC RCV000170071.1,