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

rs794728636

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794728636(-;T)
Make rs794728636(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64810052
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728636
ClinGenrs794728636
ebirs794728636
HLIrs794728636
Exacrs794728636
Varsomers794728636
Maprs794728636
PheGenIrs794728636
hapmaprs794728636
1000 genomesrs794728636
hgdprs794728636
ensemblrs794728636
gopubmedrs794728636
geneviewrs794728636
scholarrs794728636
googlers794728636
pharmgkbrs794728636
gwascentralrs794728636
openSNPrs794728636
23andMers794728636
23andMe allrs794728636
SNP Nexus

SNPshotrs794728636
SNPdbers794728636
MSV3drs794728636
GWAS Ctlgrs794728636
Max Magnitude0
ClinVar
Risk rs794728636(T;T)
Alt rs794728636(T;T)
Reference Rs794728636(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64577524_64577525insA
CLNSRC
CLNACC RCV000182430.1,