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rs587776841

From SNPedia

Orientationplus
Stabilizedminus
Geno Mag Summary
(-;GTCT) 5.8 Multiple Endocrine Neoplasia Type 1
(AGAC;AGAC) 0 common in clinvar
(GTCT;GTCT) 0 common in clinvar
(I;I) 0 common genotype
Make rs587776841(-;-)
Make rs587776841(-;AGAC)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position64809858
GeneMEN1
is asnp
is mentioned by
dbSNPrs587776841
dbSNP (classic)rs587776841
ClinGenrs587776841
ebirs587776841
HLIrs587776841
Exacrs587776841
Gnomadrs587776841
Varsomers587776841
LitVarrs587776841
Maprs587776841
PheGenIrs587776841
Biobankrs587776841
1000 genomesrs587776841
hgdprs587776841
ensemblrs587776841
geneviewrs587776841
scholarrs587776841
googlers587776841
pharmgkbrs587776841
gwascentralrs587776841
openSNPrs587776841
23andMers587776841
SNPshotrs587776841
SNPdbers587776841
MSV3drs587776841
GWAS Ctlgrs587776841
Max Magnitude5.8
ClinVar
Risk Rs587776841(AGAC;AGAC) rs587776841(-;-)
Alt Rs587776841(AGAC;AGAC) rs587776841(-;-)
Reference Rs587776841(GTCT;GTCT)
Significance Pathogenic
Disease Lipoma not provided Multiple endocrine neoplasia Hereditary cancer-predisposing syndrome
Variation info
Gene MEN1
CLNDBN Lipoma, somatic not provided Multiple endocrine neoplasia, type 1 Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000011.9:g.64577330_64577333delAGAC
CLNSRC OMIM Allelic Variant
CLNACC RCV000018173.4, RCV000182434.2, RCV000206170.3, RCV000491114.1,