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rs121917832

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121917832(A;A)
Make rs121917832(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position12718066
GeneCDKN1B
is asnp
is mentioned by
dbSNPrs121917832
ebirs121917832
HLIrs121917832
Exacrs121917832
Varsomers121917832
Maprs121917832
PheGenIrs121917832
hapmaprs121917832
1000 genomesrs121917832
hgdprs121917832
ensemblrs121917832
gopubmedrs121917832
geneviewrs121917832
scholarrs121917832
googlers121917832
pharmgkbrs121917832
gwascentralrs121917832
openSNPrs121917832
23andMers121917832
23andMe allrs121917832
SNP Nexus

SNPshotrs121917832
SNPdbers121917832
MSV3drs121917832
GWAS Ctlgrs121917832
Max Magnitude0
ClinVar
Risk rs121917832(A;A)
Alt rs121917832(A;A)
Reference rs121917832(G;G)
Significance Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene LOC101929220 CDKN1B
CLNDBN Multiple endocrine neoplasia, type 4
Reversed 0
HGVS NC_000012.11:g.12871000G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009371.4,



[PMID 26579581] Genetic and environmental predictors of chronic kidney disease in patients with type 2 diabetes and diabetic foot ulcer: a pilot study