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rs796052461

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052461(C;T)
Make rs796052461(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767824
GeneFOXG1
is asnp
is mentioned by
dbSNPrs796052461
ebirs796052461
HLIrs796052461
Exacrs796052461
Varsomers796052461
Maprs796052461
PheGenIrs796052461
hapmaprs796052461
1000 genomesrs796052461
hgdprs796052461
ensemblrs796052461
gopubmedrs796052461
geneviewrs796052461
scholarrs796052461
googlers796052461
pharmgkbrs796052461
gwascentralrs796052461
openSNPrs796052461
23andMers796052461
23andMe allrs796052461
SNP Nexus

SNPshotrs796052461
SNPdbers796052461
MSV3drs796052461
GWAS Ctlgrs796052461
Max Magnitude0
ClinVar
Risk rs796052461(T;T)
Alt rs796052461(T;T)
Reference rs796052461(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29237030C>T
CLNSRC
CLNACC RCV000187455.1,