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rs758966293

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs758966293(C;T)
Make rs758966293(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position126275377
GeneFOXRED1
is asnp
is mentioned by
dbSNPrs758966293
ebirs758966293
HLIrs758966293
Exacrs758966293
Varsomers758966293
Maprs758966293
PheGenIrs758966293
hapmaprs758966293
1000 genomesrs758966293
hgdprs758966293
ensemblrs758966293
gopubmedrs758966293
geneviewrs758966293
scholarrs758966293
googlers758966293
pharmgkbrs758966293
gwascentralrs758966293
openSNPrs758966293
23andMers758966293
23andMe allrs758966293
SNP Nexus

SNPshotrs758966293
SNPdbers758966293
MSV3drs758966293
GWAS Ctlgrs758966293
Max Magnitude0
ClinVar
Risk rs758966293(T;T)
Alt rs758966293(T;T)
Reference rs758966293(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FOXRED1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.126145272C>T
CLNSRC
CLNACC RCV000195921.1,