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rs386134259

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs386134259(A;A)
Make rs386134259(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position64807577
GeneMEN1
is asnp
is mentioned by
dbSNPrs386134259
ebirs386134259
HLIrs386134259
Exacrs386134259
Varsomers386134259
Maprs386134259
PheGenIrs386134259
hapmaprs386134259
1000 genomesrs386134259
hgdprs386134259
ensemblrs386134259
gopubmedrs386134259
geneviewrs386134259
scholarrs386134259
googlers386134259
pharmgkbrs386134259
gwascentralrs386134259
openSNPrs386134259
23andMers386134259
23andMe allrs386134259
SNP Nexus

SNPshotrs386134259
SNPdbers386134259
MSV3drs386134259
GWAS Ctlgrs386134259
Max Magnitude0
ClinVar
Risk rs386134259(A,T;A,T)
Alt rs386134259(A,T;A,T)
Reference rs386134259(C;C)
Significance Pathogenic
Disease not provided Multiple endocrine neoplasia
Variation info
Gene MEN1
CLNDBN not provided Multiple endocrine neoplasia, type 1
Reversed 1
HGVS NC_000011.9:g.64575049G>A; NC_000011.9:g.64575049G>T
CLNSRC ClinVar
CLNACC RCV000182452.1, RCV000030209.1,