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rs386134248

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TGCTGG;TGCTGG) 0 common in clinvar
Make rs386134248(-;-)
Make rs386134248(-;TGCTGG)
ReferenceGRCh38 38.1/141
Chromosome11
Position64809986
GeneMEN1
is asnp
is mentioned by
dbSNPrs386134248
ebirs386134248
HLIrs386134248
Exacrs386134248
Varsomers386134248
Maprs386134248
PheGenIrs386134248
hapmaprs386134248
1000 genomesrs386134248
hgdprs386134248
ensemblrs386134248
gopubmedrs386134248
geneviewrs386134248
scholarrs386134248
googlers386134248
pharmgkbrs386134248
gwascentralrs386134248
openSNPrs386134248
23andMers386134248
23andMe allrs386134248
SNP Nexus

SNPshotrs386134248
SNPdbers386134248
MSV3drs386134248
GWAS Ctlgrs386134248
Max Magnitude0
ClinVar
Risk rs386134248(;)
Alt rs386134248(;)
Reference rs386134248(TGCTGG;TGCTGG)
Significance Probable-Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene MEN1
CLNDBN Multiple endocrine neoplasia, type 1
Reversed 1
HGVS NC_000011.9:g.64577458_64577463delCCAGCA
CLNSRC ClinVar
CLNACC RCV000030195.1,