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rs1060499976

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499976(G;T)
Make rs1060499976(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position64807178
GeneMEN1
is asnp
is mentioned by
dbSNPrs1060499976
dbSNP (old)rs1060499976
ClinGenrs1060499976
ebirs1060499976
HLIrs1060499976
Exacrs1060499976
Gnomadrs1060499976
Varsomers1060499976
Maprs1060499976
PheGenIrs1060499976
Biobankrs1060499976
1000 genomesrs1060499976
hgdprs1060499976
ensemblrs1060499976
gopubmedrs1060499976
geneviewrs1060499976
scholarrs1060499976
googlers1060499976
pharmgkbrs1060499976
gwascentralrs1060499976
openSNPrs1060499976
23andMers1060499976
23andMe allrs1060499976
SNPshotrs1060499976
SNPdbers1060499976
MSV3drs1060499976
GWAS Ctlgrs1060499976
Max Magnitude0
ClinVar
Risk rs1060499976(C;C) rs1060499976(T;T)
Alt rs1060499976(C;C) rs1060499976(T;T)
Reference Rs1060499976(G;G)
Significance Pathogenic
Disease Multiple endocrine neoplasia Hereditary cancer-predisposing syndrome
Variation info
Gene MEN1
CLNDBN Multiple endocrine neoplasia, type 1 Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000011.9:g.64574650C>A; NC_000011.9:g.64574650C>G
CLNSRC
CLNACC RCV000466988.1, RCV000491420.1,