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rs5030952

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0
Make rs5030952(C;T)
Make rs5030952(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240603286
GeneCAPN10
is asnp
is mentioned by
dbSNPrs5030952
ebirs5030952
HLIrs5030952
Exacrs5030952
Varsomers5030952
Maprs5030952
PheGenIrs5030952
hapmaprs5030952
1000 genomesrs5030952
hgdprs5030952
ensemblrs5030952
gopubmedrs5030952
geneviewrs5030952
scholarrs5030952
googlers5030952
pharmgkbrs5030952
gwascentralrs5030952
openSNPrs5030952
23andMers5030952
23andMe allrs5030952
SNP Nexus

SNPshotrs5030952
SNPdbers5030952
MSV3drs5030952
GWAS Ctlgrs5030952
GMAF0.2378
Max Magnitude0
OMIM605286
DescCALPAIN 10; CAPN10
Variant
Relatedalso


[PMID 19752882] Association of calpain-10 gene polymorphism and posttransplant diabetes mellitus in kidney transplant patients medicated with tacrolimus



[PMID 20470430OA-icon.png] Common polymorphisms of calpain-10 and the risk of Type 2 Diabetes in a Tunisian Arab population: a case-control study

OMIM605286
Desc
Variant0003
Relatedalso
[PMID 22384174OA-icon.png] Association of CAPN10 SNPs and Haplotypes with Polycystic Ovary Syndrome among South Indian Women


[PMID 14730479OA-icon.png] Are variants in the CAPN10 gene related to risk of type 2 diabetes? A quantitative assessment of population and family-based association studies.


[PMID 18603647OA-icon.png] Functional genetic polymorphisms and female reproductive disorders: Part I: Polycystic ovary syndrome and ovarian response.


[PMID 19193380OA-icon.png] Replication of calpain-10 genetic association with carotid intima-media thickness.


[PMID 19387820OA-icon.png] Genetic polymorphisms of FSHR, CYP17, CYP1A1, CAPN10, INSR, SERPINE1 genes in adolescent girls with polycystic ovary syndrome.


[PMID 20119856] Haplotype association of calpain 10 gene variants with type 2 diabetes mellitus in an Irish sample.


[PMID 20667559] Association of calpain 10 gene polymorphisms with type 2 diabetes mellitus in Southern Indians.


GET Evidence
rs5030952
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.206349
summary



[PMID 24612564] Association of IRS-1, CAPN10 and PPARG gene polymorphisms with T2DM in the high risk population of Hyderabad, India


[PMID 27324783] Meta-analysis of the association between four CAPN10 gene variants and gestational diabetes mellitus.