Have questions? Visit https://www.reddit.com/r/SNPedia

rs121913035

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913035(A;T)
Make rs121913035(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position64804513
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs121913035
ebirs121913035
HLIrs121913035
Exacrs121913035
Varsomers121913035
Maprs121913035
PheGenIrs121913035
hapmaprs121913035
1000 genomesrs121913035
hgdprs121913035
ensemblrs121913035
gopubmedrs121913035
geneviewrs121913035
scholarrs121913035
googlers121913035
pharmgkbrs121913035
gwascentralrs121913035
openSNPrs121913035
23andMers121913035
23andMe allrs121913035
SNP Nexus

SNPshotrs121913035
SNPdbers121913035
MSV3drs121913035
GWAS Ctlgrs121913035
Max Magnitude0
ClinVar
Risk rs121913035(T;T)
Alt rs121913035(T;T)
Reference rs121913035(A;A)
Significance Pathogenic
Disease Adenoma of the adrenal gland
Variation info
Gene MAP4K2 MEN1
CLNDBN Adenoma of the adrenal gland
Reversed 1
HGVS NC_000011.9:g.64571985T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018178.4,