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rs3750965

From SNPedia

Orientationplus
Stabilizedplus
Make rs3750965(A;A)
Make rs3750965(A;G)
Make rs3750965(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position69072692
GeneTPCN2
is asnp
is mentioned by
dbSNPrs3750965
ebirs3750965
HLIrs3750965
Exacrs3750965
Varsomers3750965
Maprs3750965
PheGenIrs3750965
hapmaprs3750965
1000 genomesrs3750965
hgdprs3750965
ensemblrs3750965
gopubmedrs3750965
geneviewrs3750965
scholarrs3750965
googlers3750965
pharmgkbrs3750965
gwascentralrs3750965
openSNPrs3750965
23andMers3750965
23andMe allrs3750965
SNP Nexus

SNPshotrs3750965
SNPdbers3750965
MSV3drs3750965
GWAS Ctlgrs3750965
GMAF0.2548
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20585627OA-icon.png]
Trait Hair color
Title Web-based, participant-driven studies yield novel genetic associations for common traits
Risk Allele
P-val 3E-7
Odds Ratio None None


GET Evidence
TPCN2-K376R
aa_change Lys376Arg
aa_change_short K376R
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.290482
summary



[PMID 26918892] Genetic Variants of TPCN2 Associated with Type 2 Diabetes Risk in the Chinese Population.