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rs1060499981

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499981(A;A)
Make rs1060499981(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position64805056
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs1060499981
dbSNP (old)rs1060499981
ClinGenrs1060499981
ebirs1060499981
HLIrs1060499981
Exacrs1060499981
Gnomadrs1060499981
Varsomers1060499981
Maprs1060499981
PheGenIrs1060499981
Biobankrs1060499981
1000 genomesrs1060499981
hgdprs1060499981
ensemblrs1060499981
gopubmedrs1060499981
geneviewrs1060499981
scholarrs1060499981
googlers1060499981
pharmgkbrs1060499981
gwascentralrs1060499981
openSNPrs1060499981
23andMers1060499981
23andMe allrs1060499981
SNPshotrs1060499981
SNPdbers1060499981
MSV3drs1060499981
GWAS Ctlgrs1060499981
Max Magnitude0
ClinVar
Risk rs1060499981(A;A)
Alt rs1060499981(A;A)
Reference Rs1060499981(C;C)
Significance Probable-Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene MAP4K2 MEN1
CLNDBN Multiple endocrine neoplasia, type 1
Reversed 1
HGVS NC_000011.9:g.64572528G>T
CLNSRC
CLNACC RCV000467767.1,