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rs1060499987

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060499987(A;A)
Make rs1060499987(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position64809792
GeneMEN1
is asnp
is mentioned by
dbSNPrs1060499987
dbSNP (old)rs1060499987
ClinGenrs1060499987
ebirs1060499987
HLIrs1060499987
Exacrs1060499987
Gnomadrs1060499987
Varsomers1060499987
Maprs1060499987
PheGenIrs1060499987
Biobankrs1060499987
1000 genomesrs1060499987
hgdprs1060499987
ensemblrs1060499987
gopubmedrs1060499987
geneviewrs1060499987
scholarrs1060499987
googlers1060499987
pharmgkbrs1060499987
gwascentralrs1060499987
openSNPrs1060499987
23andMers1060499987
23andMe allrs1060499987
SNPshotrs1060499987
SNPdbers1060499987
MSV3drs1060499987
GWAS Ctlgrs1060499987
Max Magnitude0
ClinVar
Risk rs1060499987(A;A)
Alt rs1060499987(A;A)
Reference Rs1060499987(T;T)
Significance Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene MEN1
CLNDBN Multiple endocrine neoplasia, type 1
Reversed 1
HGVS NC_000011.9:g.64577264A>T
CLNSRC
CLNACC RCV000472445.1,