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rs761695866

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs761695866(-;C)
Make rs761695866(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64804618
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs761695866
dbSNP (old)rs761695866
ClinGenrs761695866
ebirs761695866
HLIrs761695866
Exacrs761695866
Varsomers761695866
Maprs761695866
PheGenIrs761695866
Biobankrs761695866
1000 genomesrs761695866
hgdprs761695866
ensemblrs761695866
gopubmedrs761695866
geneviewrs761695866
scholarrs761695866
googlers761695866
pharmgkbrs761695866
gwascentralrs761695866
openSNPrs761695866
23andMers761695866
23andMe allrs761695866
SNP Nexus

SNPshotrs761695866
SNPdbers761695866
MSV3drs761695866
GWAS Ctlgrs761695866
Max Magnitude0
ClinVar
Risk rs761695866(C;C)
Alt rs761695866(C;C)
Reference Rs761695866(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene MAP4K2 MEN1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.64572091dupC
CLNSRC
CLNACC RCV000182442.1,