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rs2975766

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs2975766(A;A)
Make rs2975766(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240598657
GeneCAPN10
is asnp
is mentioned by
dbSNPrs2975766
ebirs2975766
HLIrs2975766
Exacrs2975766
Varsomers2975766
Maprs2975766
PheGenIrs2975766
hapmaprs2975766
1000 genomesrs2975766
hgdprs2975766
ensemblrs2975766
gopubmedrs2975766
geneviewrs2975766
scholarrs2975766
googlers2975766
pharmgkbrs2975766
gwascentralrs2975766
openSNPrs2975766
23andMers2975766
23andMe allrs2975766
SNP Nexus

SNPshotrs2975766
SNPdbers2975766
MSV3drs2975766
GWAS Ctlgrs2975766
GMAF0.01331
Max Magnitude0
? (A;A) (A;G) (G;G) 28
Venter snp
Source plos
Gene CAPN10
allele G
frequency 0.975
sift TOLERATED
HuRef 1103658409726
Disease Association Defects in CAPN10 are associated with type II diabetes (NIDDM) (MIM:125853).



[PMID 19416960OA-icon.png] Mouse population-guided resequencing reveals that variants in CD44 contribute to acetaminophen-induced liver injury in humans.


GET Evidence
CAPN10-I666V
aa_change Ile666Val
aa_change_short I666V
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.97864
summary