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rs386134251

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CC;CC) 0 common in clinvar
Make rs386134251(-;-)
Make rs386134251(-;CC)
ReferenceGRCh38 38.1/141
Chromosome11
Position64809898
GeneMEN1
is asnp
is mentioned by
dbSNPrs386134251
ebirs386134251
HLIrs386134251
Exacrs386134251
Varsomers386134251
Maprs386134251
PheGenIrs386134251
hapmaprs386134251
1000 genomesrs386134251
hgdprs386134251
ensemblrs386134251
gopubmedrs386134251
geneviewrs386134251
scholarrs386134251
googlers386134251
pharmgkbrs386134251
gwascentralrs386134251
openSNPrs386134251
23andMers386134251
23andMe allrs386134251
SNP Nexus

SNPshotrs386134251
SNPdbers386134251
MSV3drs386134251
GWAS Ctlgrs386134251
Max Magnitude0
ClinVar
Risk rs386134251(;)
Alt rs386134251(;)
Reference rs386134251(CC;CC)
Significance Pathogenic
Disease Multiple endocrine neoplasia not provided
Variation info
Gene MEN1
CLNDBN Multiple endocrine neoplasia, type 1 not provided
Reversed 1
HGVS NC_000011.9:g.64577370_64577371delGG
CLNSRC ClinVar LabCorp
CLNACC RCV000030199.2, RCV000182433.1,