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rs745404679

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs745404679(A;A)
Make rs745404679(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64804549
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs745404679
ebirs745404679
HLIrs745404679
Exacrs745404679
Varsomers745404679
Maprs745404679
PheGenIrs745404679
hapmaprs745404679
1000 genomesrs745404679
hgdprs745404679
ensemblrs745404679
gopubmedrs745404679
geneviewrs745404679
scholarrs745404679
googlers745404679
pharmgkbrs745404679
gwascentralrs745404679
openSNPrs745404679
23andMers745404679
23andMe allrs745404679
SNP Nexus

SNPshotrs745404679
SNPdbers745404679
MSV3drs745404679
GWAS Ctlgrs745404679
Max Magnitude0
ClinVar
Risk rs745404679(A,T;A,T)
Alt rs745404679(A,T;A,T)
Reference rs745404679(G;G)
Significance Pathogenic
Disease not provided Multiple endocrine neoplasia
Variation info
Gene MAP4K2 MEN1
CLNDBN not provided Multiple endocrine neoplasia, type 1
Reversed 0
HGVS NC_000011.9:g.64572021G>A
CLNSRC
CLNACC RCV000182424.1, RCV000231689.1,