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rs794728644

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GTGAGGGACAG;GTGAGGGACAG) 0 common in clinvar
Make rs794728644(-;-)
Make rs794728644(-;GTGAGGGACAG)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64805023
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs794728644
dbSNP (old)rs794728644
ClinGenrs794728644
ebirs794728644
HLIrs794728644
Exacrs794728644
Varsomers794728644
Maprs794728644
PheGenIrs794728644
Biobankrs794728644
1000 genomesrs794728644
hgdprs794728644
ensemblrs794728644
gopubmedrs794728644
geneviewrs794728644
scholarrs794728644
googlers794728644
pharmgkbrs794728644
gwascentralrs794728644
openSNPrs794728644
23andMers794728644
23andMe allrs794728644
SNP Nexus

SNPshotrs794728644
SNPdbers794728644
MSV3drs794728644
GWAS Ctlgrs794728644
Max Magnitude0
ClinVar
Risk rs794728644(-;-)
Alt rs794728644(-;-)
Reference Rs794728644(GTGAGGGACAG;GTGAGGGACAG)
Significance Pathogenic
Disease not provided
Variation info
Gene MAP4K2 MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64572495_64572505delCTGTCCCTCAC
CLNSRC
CLNACC RCV000182441.1,