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rs386134261

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs386134261(-;-)
Make rs386134261(-;T)
Make rs386134261(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position64806325
GeneMEN1
is asnp
is mentioned by
dbSNPrs386134261
ebirs386134261
HLIrs386134261
Exacrs386134261
Varsomers386134261
Maprs386134261
PheGenIrs386134261
hapmaprs386134261
1000 genomesrs386134261
hgdprs386134261
ensemblrs386134261
gopubmedrs386134261
geneviewrs386134261
scholarrs386134261
googlers386134261
pharmgkbrs386134261
gwascentralrs386134261
openSNPrs386134261
23andMers386134261
23andMe allrs386134261
SNP Nexus

SNPshotrs386134261
SNPdbers386134261
MSV3drs386134261
GWAS Ctlgrs386134261
Max Magnitude0
ClinVar
Risk rs386134261(T;T)
Alt rs386134261(T;T)
Reference rs386134261(;)
Significance Probable-Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene MEN1
CLNDBN Multiple endocrine neoplasia, type 1
Reversed 1
HGVS NC_000011.9:g.64573798dupA
CLNSRC ClinVar LabCorp
CLNACC RCV000030211.1,