Have questions? Visit https://www.reddit.com/r/SNPedia

rs794728647

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728647(C;T)
Make rs794728647(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64809788
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728647
ebirs794728647
HLIrs794728647
Exacrs794728647
Varsomers794728647
Maprs794728647
PheGenIrs794728647
hapmaprs794728647
1000 genomesrs794728647
hgdprs794728647
ensemblrs794728647
gopubmedrs794728647
geneviewrs794728647
scholarrs794728647
googlers794728647
pharmgkbrs794728647
gwascentralrs794728647
openSNPrs794728647
23andMers794728647
23andMe allrs794728647
SNP Nexus

SNPshotrs794728647
SNPdbers794728647
MSV3drs794728647
GWAS Ctlgrs794728647
Max Magnitude0
ClinVar
Risk rs794728647(T;T)
Alt rs794728647(T;T)
Reference rs794728647(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64577260G>A
CLNSRC
CLNACC RCV000182446.2,