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

rs794728661

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AGA;AGA) 0 common in clinvar
Make rs794728661(-;-)
Make rs794728661(-;AGA)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64804495
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs794728661
ClinGenrs794728661
ebirs794728661
HLIrs794728661
Exacrs794728661
Varsomers794728661
Maprs794728661
PheGenIrs794728661
hapmaprs794728661
1000 genomesrs794728661
hgdprs794728661
ensemblrs794728661
gopubmedrs794728661
geneviewrs794728661
scholarrs794728661
googlers794728661
pharmgkbrs794728661
gwascentralrs794728661
openSNPrs794728661
23andMers794728661
23andMe allrs794728661
SNP Nexus

SNPshotrs794728661
SNPdbers794728661
MSV3drs794728661
GWAS Ctlgrs794728661
Max Magnitude0
ClinVar
Risk rs794728661(-;-)
Alt rs794728661(-;-)
Reference Rs794728661(AGA;AGA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MAP4K2 MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64571967_64571969delTCT
CLNSRC
CLNACC RCV000182464.2,