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rs794728637

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CTGGGCCGAG;CTGGGCCGAG) 0 common in clinvar
Make rs794728637(-;-)
Make rs794728637(-;CTGGGCCGAG)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64810022
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728637
dbSNP (old)rs794728637
ClinGenrs794728637
ebirs794728637
HLIrs794728637
Exacrs794728637
Gnomadrs794728637
Varsomers794728637
Maprs794728637
PheGenIrs794728637
Biobankrs794728637
1000 genomesrs794728637
hgdprs794728637
ensemblrs794728637
gopubmedrs794728637
geneviewrs794728637
scholarrs794728637
googlers794728637
pharmgkbrs794728637
gwascentralrs794728637
openSNPrs794728637
23andMers794728637
23andMe allrs794728637
SNP Nexus

SNPshotrs794728637
SNPdbers794728637
MSV3drs794728637
GWAS Ctlgrs794728637
Max Magnitude0
ClinVar
Risk rs794728637(-;-)
Alt rs794728637(-;-)
Reference Rs794728637(CTGGGCCGAG;CTGGGCCGAG)
Significance Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64577494_64577503delCTCGGCCCAG
CLNSRC
CLNACC RCV000182431.1,