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rs794728656

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794728656(-;C)
Make rs794728656(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64809945
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728656
dbSNP (old)rs794728656
ClinGenrs794728656
ebirs794728656
HLIrs794728656
Exacrs794728656
Gnomadrs794728656
Varsomers794728656
Maprs794728656
PheGenIrs794728656
Biobankrs794728656
1000 genomesrs794728656
hgdprs794728656
ensemblrs794728656
gopubmedrs794728656
geneviewrs794728656
scholarrs794728656
googlers794728656
pharmgkbrs794728656
gwascentralrs794728656
openSNPrs794728656
23andMers794728656
23andMe allrs794728656
SNP Nexus

SNPshotrs794728656
SNPdbers794728656
MSV3drs794728656
GWAS Ctlgrs794728656
Max Magnitude0
ClinVar
Risk rs794728656(C;C)
Alt rs794728656(C;C)
Reference Rs794728656(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64577418dupG
CLNSRC
CLNACC RCV000182458.1,