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rs794728620

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728620(C;T)
Make rs794728620(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64807893
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728620
ebirs794728620
HLIrs794728620
Exacrs794728620
Varsomers794728620
Maprs794728620
PheGenIrs794728620
hapmaprs794728620
1000 genomesrs794728620
hgdprs794728620
ensemblrs794728620
gopubmedrs794728620
geneviewrs794728620
scholarrs794728620
googlers794728620
pharmgkbrs794728620
gwascentralrs794728620
openSNPrs794728620
23andMers794728620
23andMe allrs794728620
SNP Nexus

SNPshotrs794728620
SNPdbers794728620
MSV3drs794728620
GWAS Ctlgrs794728620
Max Magnitude0
ClinVar
Risk rs794728620(T;T)
Alt rs794728620(T;T)
Reference rs794728620(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64575365G>A
CLNSRC
CLNACC RCV000182409.1,