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rs794728641

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(ACATCTAC;ACATCTAC) 0 common in clinvar
Make rs794728641(-;-)
Make rs794728641(-;ACATCTAC)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64806324
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728641
dbSNP (old)rs794728641
ClinGenrs794728641
ebirs794728641
HLIrs794728641
Exacrs794728641
Gnomadrs794728641
Varsomers794728641
Maprs794728641
PheGenIrs794728641
Biobankrs794728641
1000 genomesrs794728641
hgdprs794728641
ensemblrs794728641
gopubmedrs794728641
geneviewrs794728641
scholarrs794728641
googlers794728641
pharmgkbrs794728641
gwascentralrs794728641
openSNPrs794728641
23andMers794728641
23andMe allrs794728641
SNP Nexus

SNPshotrs794728641
SNPdbers794728641
MSV3drs794728641
GWAS Ctlgrs794728641
Max Magnitude0
ClinVar
Risk rs794728641(-;-)
Alt rs794728641(-;-)
Reference Rs794728641(ACATCTAC;ACATCTAC)
Significance Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64573796_64573803delGTAGATGT
CLNSRC
CLNACC RCV000182438.1,