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rs794728655

From SNPedia

Orientationminus
Make rs794728655(-;-)
Make rs794728655(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64810055
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728655
ebirs794728655
HLIrs794728655
Exacrs794728655
Varsomers794728655
Maprs794728655
PheGenIrs794728655
hapmaprs794728655
1000 genomesrs794728655
hgdprs794728655
ensemblrs794728655
gopubmedrs794728655
geneviewrs794728655
scholarrs794728655
googlers794728655
pharmgkbrs794728655
gwascentralrs794728655
openSNPrs794728655
23andMers794728655
23andMe allrs794728655
SNP Nexus

SNPshotrs794728655
SNPdbers794728655
MSV3drs794728655
GWAS Ctlgrs794728655
Max Magnitude
ClinVar
Risk rs794728655(;)
Alt rs794728655(;)
Reference rs794728655(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64577527delC
CLNSRC
CLNACC RCV000182457.1,