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rs794728660

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794728660(-;GGCTCAGGTGCCAGCAC)
Make rs794728660(GGCTCAGGTGCCAGCAC;GGCTCAGGTGCCAGCAC)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64804548
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs794728660
dbSNP (old)rs794728660
ClinGenrs794728660
ebirs794728660
HLIrs794728660
Exacrs794728660
Gnomadrs794728660
Varsomers794728660
Maprs794728660
PheGenIrs794728660
Biobankrs794728660
1000 genomesrs794728660
hgdprs794728660
ensemblrs794728660
gopubmedrs794728660
geneviewrs794728660
scholarrs794728660
googlers794728660
pharmgkbrs794728660
gwascentralrs794728660
openSNPrs794728660
23andMers794728660
23andMe allrs794728660
SNP Nexus

SNPshotrs794728660
SNPdbers794728660
MSV3drs794728660
GWAS Ctlgrs794728660
Max Magnitude0
ClinVar
Risk rs794728660(GGCTCAGGTGCCAGCAC;GGCTCAGGTGCCAGCAC)
Alt rs794728660(GGCTCAGGTGCCAGCAC;GGCTCAGGTGCCAGCAC)
Reference Rs794728660(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene MAP4K2 MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64572021_64572037dup17
CLNSRC
CLNACC RCV000182463.1,