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rs3737965

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs3737965(C;T)
Make rs3737965(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position11806394
GeneCLCN6, MTHFR
is asnp
is mentioned by
dbSNPrs3737965
ebirs3737965
HLIrs3737965
Exacrs3737965
Varsomers3737965
Maprs3737965
PheGenIrs3737965
hapmaprs3737965
1000 genomesrs3737965
hgdprs3737965
ensemblrs3737965
gopubmedrs3737965
geneviewrs3737965
scholarrs3737965
googlers3737965
pharmgkbrs3737965
gwascentralrs3737965
openSNPrs3737965
23andMers3737965
23andMe allrs3737965
SNP Nexus

SNPshotrs3737965
SNPdbers3737965
MSV3drs3737965
GWAS Ctlgrs3737965
GMAF0.05188
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GET Evidence
rs3737965
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0305042
summary



[PMID 26740945] The rs3737964 single-nucleotide polymorphism of the chloride channel-6 gene as a risk factor for coronary heart disease.