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rs794728622

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728622(G;T)
Make rs794728622(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64807890
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728622
ebirs794728622
HLIrs794728622
Exacrs794728622
Varsomers794728622
Maprs794728622
PheGenIrs794728622
hapmaprs794728622
1000 genomesrs794728622
hgdprs794728622
ensemblrs794728622
gopubmedrs794728622
geneviewrs794728622
scholarrs794728622
googlers794728622
pharmgkbrs794728622
gwascentralrs794728622
openSNPrs794728622
23andMers794728622
23andMe allrs794728622
SNP Nexus

SNPshotrs794728622
SNPdbers794728622
MSV3drs794728622
GWAS Ctlgrs794728622
Max Magnitude0
ClinVar
Risk rs794728622(T;T)
Alt rs794728622(T;T)
Reference rs794728622(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64575362C>A
CLNSRC
CLNACC RCV000182411.1,