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rs794728618

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728618(A;T)
Make rs794728618(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64808030
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728618
ebirs794728618
HLIrs794728618
Exacrs794728618
Varsomers794728618
Maprs794728618
PheGenIrs794728618
hapmaprs794728618
1000 genomesrs794728618
hgdprs794728618
ensemblrs794728618
gopubmedrs794728618
geneviewrs794728618
scholarrs794728618
googlers794728618
pharmgkbrs794728618
gwascentralrs794728618
openSNPrs794728618
23andMers794728618
23andMe allrs794728618
SNP Nexus

SNPshotrs794728618
SNPdbers794728618
MSV3drs794728618
GWAS Ctlgrs794728618
Max Magnitude0
ClinVar
Risk rs794728618(T;T)
Alt rs794728618(T;T)
Reference rs794728618(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64575502T>A
CLNSRC
CLNACC RCV000182406.1,