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rs12635698

From SNPedia

Orientationplus
Stabilizedplus
Make rs12635698(C;C)
Make rs12635698(C;T)
Make rs12635698(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position16366982
GeneRFTN1
is asnp
is mentioned by
dbSNPrs12635698
ebirs12635698
HLIrs12635698
Exacrs12635698
Varsomers12635698
Maprs12635698
PheGenIrs12635698
hapmaprs12635698
1000 genomesrs12635698
hgdprs12635698
ensemblrs12635698
gopubmedrs12635698
geneviewrs12635698
scholarrs12635698
googlers12635698
pharmgkbrs12635698
gwascentralrs12635698
openSNPrs12635698
23andMers12635698
23andMe allrs12635698
SNP Nexus

SNPshotrs12635698
SNPdbers12635698
MSV3drs12635698
GWAS Ctlgrs12635698
GMAF0.208
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19553259OA-icon.png]
Trait Obesity (extreme)
Title Common BMI-associated variants confer risk of extreme obesity
Risk Allele C
P-val 0.000005
Odds Ratio 1.41 [1.21-1.63]


GET Evidence
rs12635698
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.28125
summary



Occurs within the RFTN1 (Raftlin, lipid raft linker 1) gene