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rs796052477

From SNPedia

Orientationplus
Make rs796052477(-;-)
Make rs796052477(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767678
GeneFOXG1
is asnp
is mentioned by
dbSNPrs796052477
ebirs796052477
HLIrs796052477
Exacrs796052477
Varsomers796052477
Maprs796052477
PheGenIrs796052477
hapmaprs796052477
1000 genomesrs796052477
hgdprs796052477
ensemblrs796052477
gopubmedrs796052477
geneviewrs796052477
scholarrs796052477
googlers796052477
pharmgkbrs796052477
gwascentralrs796052477
openSNPrs796052477
23andMers796052477
23andMe allrs796052477
SNP Nexus

SNPshotrs796052477
SNPdbers796052477
MSV3drs796052477
GWAS Ctlgrs796052477
Max Magnitude
ClinVar
Risk rs796052477(;)
Alt rs796052477(;)
Reference rs796052477(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29236884delG
CLNSRC
CLNACC RCV000187479.1,