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rs794728658

From SNPedia

Orientationminus
Make rs794728658(-;-)
Make rs794728658(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64805710
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728658
ebirs794728658
HLIrs794728658
Exacrs794728658
Varsomers794728658
Maprs794728658
PheGenIrs794728658
hapmaprs794728658
1000 genomesrs794728658
hgdprs794728658
ensemblrs794728658
gopubmedrs794728658
geneviewrs794728658
scholarrs794728658
googlers794728658
pharmgkbrs794728658
gwascentralrs794728658
openSNPrs794728658
23andMers794728658
23andMe allrs794728658
SNP Nexus

SNPshotrs794728658
SNPdbers794728658
MSV3drs794728658
GWAS Ctlgrs794728658
Max Magnitude
ClinVar
Risk rs794728658(;)
Alt rs794728658(;)
Reference rs794728658(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64573182delA
CLNSRC
CLNACC RCV000182461.1,