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rs1060499991

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499991(A;A)
Make rs1060499991(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position64804755
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs1060499991
dbSNP (old)rs1060499991
ClinGenrs1060499991
ebirs1060499991
HLIrs1060499991
Exacrs1060499991
Gnomadrs1060499991
Varsomers1060499991
Maprs1060499991
PheGenIrs1060499991
Biobankrs1060499991
1000 genomesrs1060499991
hgdprs1060499991
ensemblrs1060499991
gopubmedrs1060499991
geneviewrs1060499991
scholarrs1060499991
googlers1060499991
pharmgkbrs1060499991
gwascentralrs1060499991
openSNPrs1060499991
23andMers1060499991
23andMe allrs1060499991
SNPshotrs1060499991
SNPdbers1060499991
MSV3drs1060499991
GWAS Ctlgrs1060499991
Max Magnitude0
ClinVar
Risk rs1060499991(A;A)
Alt rs1060499991(A;A)
Reference Rs1060499991(G;G)
Significance Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene MAP4K2 MEN1
CLNDBN Multiple endocrine neoplasia, type 1
Reversed 1
HGVS NC_000011.9:g.64572227C>T
CLNSRC
CLNACC RCV000474300.1,