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rs1085307753

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome14
Position28768457
GeneFOXG1
is asnp
is mentioned by
dbSNPrs1085307753
dbSNP (classic)rs1085307753
ClinGenrs1085307753
ebirs1085307753
HLIrs1085307753
Exacrs1085307753
Gnomadrs1085307753
Varsomers1085307753
LitVarrs1085307753
Maprs1085307753
PheGenIrs1085307753
Biobankrs1085307753
1000 genomesrs1085307753
hgdprs1085307753
ensemblrs1085307753
geneviewrs1085307753
scholarrs1085307753
googlers1085307753
pharmgkbrs1085307753
gwascentralrs1085307753
openSNPrs1085307753
23andMers1085307753
23andMe allrs1085307753
SNPshotrs1085307753
SNPdbers1085307753
MSV3drs1085307753
GWAS Ctlgrs1085307753
Max Magnitude0
ClinVar
Risk rs1085307753(G;G)
Alt rs1085307753(G;G)
Reference Rs1085307753(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29237663C>G
CLNSRC
CLNACC RCV000489047.1,