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rs386134258

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GAGCGGGT;GAGCGGGT) 0 common in clinvar
Make rs386134258(-;-)
Make rs386134258(-;GAGCGGGT)
ReferenceGRCh38 38.1/141
Chromosome11
Position64807889
GeneMEN1
is asnp
is mentioned by
dbSNPrs386134258
ebirs386134258
HLIrs386134258
Exacrs386134258
Varsomers386134258
Maprs386134258
PheGenIrs386134258
hapmaprs386134258
1000 genomesrs386134258
hgdprs386134258
ensemblrs386134258
gopubmedrs386134258
geneviewrs386134258
scholarrs386134258
googlers386134258
pharmgkbrs386134258
gwascentralrs386134258
openSNPrs386134258
23andMers386134258
23andMe allrs386134258
SNP Nexus

SNPshotrs386134258
SNPdbers386134258
MSV3drs386134258
GWAS Ctlgrs386134258
Max Magnitude0
ClinVar
Risk rs386134258(;)
Alt rs386134258(;)
Reference rs386134258(GAGCGGGT;GAGCGGGT)
Significance Probable-Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene MEN1
CLNDBN Multiple endocrine neoplasia, type 1
Reversed 1
HGVS NC_000011.9:g.64575361_64575368delACCCGCTC
CLNSRC ClinVar
CLNACC RCV000030207.1,