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rs386134250

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs386134250(A;G)
Make rs386134250(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position64810109
GeneMEN1
is asnp
is mentioned by
dbSNPrs386134250
ebirs386134250
HLIrs386134250
Exacrs386134250
Varsomers386134250
Maprs386134250
PheGenIrs386134250
hapmaprs386134250
1000 genomesrs386134250
hgdprs386134250
ensemblrs386134250
gopubmedrs386134250
geneviewrs386134250
scholarrs386134250
googlers386134250
pharmgkbrs386134250
gwascentralrs386134250
openSNPrs386134250
23andMers386134250
23andMe allrs386134250
SNP Nexus

SNPshotrs386134250
SNPdbers386134250
MSV3drs386134250
GWAS Ctlgrs386134250
Max Magnitude0
ClinVar
Risk rs386134250(G;G)
Alt rs386134250(G;G)
Reference rs386134250(A;A)
Significance Probable-Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene MEN1
CLNDBN Multiple endocrine neoplasia, type 1
Reversed 1
HGVS NC_000011.9:g.64577581T>C
CLNSRC ClinVar LabCorp
CLNACC RCV000030198.1,