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rs2274924

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2274924(A;G)
Make rs2274924(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position74761731
GeneTRPM6
is asnp
is mentioned by
dbSNPrs2274924
dbSNP (classic)rs2274924
ClinGenrs2274924
ebirs2274924
HLIrs2274924
Exacrs2274924
Gnomadrs2274924
Varsomers2274924
LitVarrs2274924
Maprs2274924
PheGenIrs2274924
Biobankrs2274924
1000 genomesrs2274924
hgdprs2274924
ensemblrs2274924
geneviewrs2274924
scholarrs2274924
googlers2274924
pharmgkbrs2274924
gwascentralrs2274924
openSNPrs2274924
23andMers2274924
SNPshotrs2274924
SNPdbers2274924
MSV3drs2274924
GWAS Ctlgrs2274924
GMAF0.2489
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 19149903OA-icon.png] 4.9x risk of type-2 diabetes among women carriers of both the rare alleles at rs3750425 and rs2274924 when their magnesium intake was lower than 250 mg per day.



[PMID 23343670OA-icon.png] Higher Magnesium Intake Is Associated with Lower Fasting Glucose and Insulin, with No Evidence of Interaction with Select Genetic Loci, in a Meta-Analysis of 15 CHARGE Consortium Studies


ClinVar
Risk rs2274924(G;G)
Alt rs2274924(G;G)
Reference Rs2274924(A;A)
Significance Non-pathogenic
Disease Hypomagnesemia 1
Variation info
Gene TRPM6
CLNDBN Hypomagnesemia 1, intestinal
Reversed 1
HGVS NC_000009.11:g.77376647T>C
CLNSRC
CLNACC RCV000347459.1,