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

rs386134246

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs386134246(-;-)
Make rs386134246(-;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position64805757
GeneMEN1
is asnp
is mentioned by
dbSNPrs386134246
dbSNP (classic)rs386134246
ClinGenrs386134246
ebirs386134246
HLIrs386134246
Exacrs386134246
Gnomadrs386134246
Varsomers386134246
LitVarrs386134246
Maprs386134246
PheGenIrs386134246
Biobankrs386134246
1000 genomesrs386134246
hgdprs386134246
ensemblrs386134246
geneviewrs386134246
scholarrs386134246
googlers386134246
pharmgkbrs386134246
gwascentralrs386134246
openSNPrs386134246
23andMers386134246
SNPshotrs386134246
SNPdbers386134246
MSV3drs386134246
GWAS Ctlgrs386134246
Max Magnitude0
ClinVar
Risk rs386134246(-;-)
Alt rs386134246(-;-)
Reference Rs386134246(C;C)
Significance Probable-Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene MEN1
CLNDBN Multiple endocrine neoplasia, type 1
Reversed 1
HGVS NC_000011.9:g.64573229delG
CLNSRC ClinVar LabCorp
CLNACC RCV000030193.1,