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rs1060499986

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060499986(A;G)
Make rs1060499986(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position64804818
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs1060499986
dbSNP (old)rs1060499986
ClinGenrs1060499986
ebirs1060499986
HLIrs1060499986
Exacrs1060499986
Gnomadrs1060499986
Varsomers1060499986
LitVarrs1060499986
Maprs1060499986
PheGenIrs1060499986
Biobankrs1060499986
1000 genomesrs1060499986
hgdprs1060499986
ensemblrs1060499986
gopubmedrs1060499986
geneviewrs1060499986
scholarrs1060499986
googlers1060499986
pharmgkbrs1060499986
gwascentralrs1060499986
openSNPrs1060499986
23andMers1060499986
23andMe allrs1060499986
SNPshotrs1060499986
SNPdbers1060499986
MSV3drs1060499986
GWAS Ctlgrs1060499986
Max Magnitude0
ClinVar
Risk rs1060499986(G;G)
Alt rs1060499986(G;G)
Reference Rs1060499986(A;A)
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.64572290T>C
CLNSRC
CLNACC RCV000457794.1,