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rs786205006

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205006(C;T)
Make rs786205006(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767889
GeneFOXG1
is asnp
is mentioned by
dbSNPrs786205006
ebirs786205006
HLIrs786205006
Exacrs786205006
Varsomers786205006
Maprs786205006
PheGenIrs786205006
hapmaprs786205006
1000 genomesrs786205006
hgdprs786205006
ensemblrs786205006
gopubmedrs786205006
geneviewrs786205006
scholarrs786205006
googlers786205006
pharmgkbrs786205006
gwascentralrs786205006
openSNPrs786205006
23andMers786205006
23andMe allrs786205006
SNP Nexus

SNPshotrs786205006
SNPdbers786205006
MSV3drs786205006
GWAS Ctlgrs786205006
Max Magnitude0
ClinVar
Risk rs786205006(T;T)
Alt rs786205006(T;T)
Reference rs786205006(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29237095C>T
CLNSRC
CLNACC RCV000170079.1,