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rs386134247

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs386134247(-;-)
Make rs386134247(-;G)
Make rs386134247(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position64805645
GeneMEN1
is asnp
is mentioned by
dbSNPrs386134247
ebirs386134247
HLIrs386134247
Exacrs386134247
Varsomers386134247
Maprs386134247
PheGenIrs386134247
hapmaprs386134247
1000 genomesrs386134247
hgdprs386134247
ensemblrs386134247
gopubmedrs386134247
geneviewrs386134247
scholarrs386134247
googlers386134247
pharmgkbrs386134247
gwascentralrs386134247
openSNPrs386134247
23andMers386134247
23andMe allrs386134247
SNP Nexus

SNPshotrs386134247
SNPdbers386134247
MSV3drs386134247
GWAS Ctlgrs386134247
Max Magnitude0
ClinVar
Risk rs386134247(G;G)
Alt rs386134247(G;G)
Reference rs386134247(;)
Significance Probable-Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene MEN1
CLNDBN Multiple endocrine neoplasia, type 1
Reversed 1
HGVS NC_000011.9:g.64573118dupC
CLNSRC ClinVar LabCorp
CLNACC RCV000030194.1,