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rs786205486

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205486(A;T)
Make rs786205486(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767973
GeneFOXG1
is asnp
is mentioned by
dbSNPrs786205486
ebirs786205486
HLIrs786205486
Exacrs786205486
Varsomers786205486
Maprs786205486
PheGenIrs786205486
hapmaprs786205486
1000 genomesrs786205486
hgdprs786205486
ensemblrs786205486
gopubmedrs786205486
geneviewrs786205486
scholarrs786205486
googlers786205486
pharmgkbrs786205486
gwascentralrs786205486
openSNPrs786205486
23andMers786205486
23andMe allrs786205486
SNP Nexus

SNPshotrs786205486
SNPdbers786205486
MSV3drs786205486
GWAS Ctlgrs786205486
Max Magnitude0
ClinVar
Risk rs786205486(T;T)
Alt rs786205486(T;T)
Reference rs786205486(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29237179A>T
CLNSRC
CLNACC RCV000171221.1,