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rs794728652

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728652(G;T)
Make rs794728652(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64807551
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728652
ebirs794728652
HLIrs794728652
Exacrs794728652
Varsomers794728652
Maprs794728652
PheGenIrs794728652
hapmaprs794728652
1000 genomesrs794728652
hgdprs794728652
ensemblrs794728652
gopubmedrs794728652
geneviewrs794728652
scholarrs794728652
googlers794728652
pharmgkbrs794728652
gwascentralrs794728652
openSNPrs794728652
23andMers794728652
23andMe allrs794728652
SNP Nexus

SNPshotrs794728652
SNPdbers794728652
MSV3drs794728652
GWAS Ctlgrs794728652
Max Magnitude0
ClinVar
Risk rs794728652(T;T)
Alt rs794728652(T;T)
Reference rs794728652(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64575023C>A
CLNSRC
CLNACC RCV000182453.1,