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rs781028867

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common genotype
Make rs781028867(C;T)
Make rs781028867(T;T)
ReferenceGRCh38.p7 38.3/151
Chromosome16
Position53873846
GeneFTO
is asnp
is mentioned by
dbSNPrs781028867
dbSNP (classic)rs781028867
ClinGenrs781028867
ebirs781028867
HLIrs781028867
Exacrs781028867
Gnomadrs781028867
Varsomers781028867
LitVarrs781028867
Maprs781028867
PheGenIrs781028867
Biobankrs781028867
1000 genomesrs781028867
hgdprs781028867
ensemblrs781028867
geneviewrs781028867
scholarrs781028867
googlers781028867
pharmgkbrs781028867
gwascentralrs781028867
openSNPrs781028867
23andMers781028867
23andMe allrs781028867
SNPshotrs781028867
SNPdbers781028867
MSV3drs781028867
GWAS Ctlgrs781028867
Max Magnitude0

aka NM_001080432.2(FTO):c.956C>T or (p.Ser319Phe)

OMIM pathogenic variant