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rs1060503789

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060503789(C;T)
Make rs1060503789(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position64807095
GeneMEN1
is asnp
is mentioned by
dbSNPrs1060503789
dbSNP (old)rs1060503789
ClinGenrs1060503789
ebirs1060503789
HLIrs1060503789
Exacrs1060503789
Gnomadrs1060503789
Varsomers1060503789
LitVarrs1060503789
Maprs1060503789
PheGenIrs1060503789
Biobankrs1060503789
1000 genomesrs1060503789
hgdprs1060503789
ensemblrs1060503789
gopubmedrs1060503789
geneviewrs1060503789
scholarrs1060503789
googlers1060503789
pharmgkbrs1060503789
gwascentralrs1060503789
openSNPrs1060503789
23andMers1060503789
23andMe allrs1060503789
SNPshotrs1060503789
SNPdbers1060503789
MSV3drs1060503789
GWAS Ctlgrs1060503789
Max Magnitude0
ClinVar
Risk rs1060503789(A;A) rs1060503789(T;T)
Alt rs1060503789(A;A) rs1060503789(T;T)
Reference Rs1060503789(C;C)
Significance Pathogenic
Disease Multiple endocrine neoplasia not provided Hereditary cancer-predisposing syndrome
Variation info
Gene MEN1
CLNDBN Multiple endocrine neoplasia, type 1 not provided Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000011.9:g.64574567G>A; NC_000011.9:g.64574567G>T
CLNSRC
CLNACC RCV000456598.1, RCV000484977.1, RCV000491793.1,