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rs1060499984

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499984(C;G)
Make rs1060499984(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position64805643
GeneMEN1
is asnp
is mentioned by
dbSNPrs1060499984
dbSNP (classic)rs1060499984
ClinGenrs1060499984
ebirs1060499984
HLIrs1060499984
Exacrs1060499984
Gnomadrs1060499984
Varsomers1060499984
LitVarrs1060499984
Maprs1060499984
PheGenIrs1060499984
Biobankrs1060499984
1000 genomesrs1060499984
hgdprs1060499984
ensemblrs1060499984
geneviewrs1060499984
scholarrs1060499984
googlers1060499984
pharmgkbrs1060499984
gwascentralrs1060499984
openSNPrs1060499984
23andMers1060499984
23andMe allrs1060499984
SNPshotrs1060499984
SNPdbers1060499984
MSV3drs1060499984
GWAS Ctlgrs1060499984
Max Magnitude0
ClinVar
Risk rs1060499984(G;G) rs1060499984(T;T)
Alt rs1060499984(G;G) rs1060499984(T;T)
Reference Rs1060499984(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Multiple endocrine neoplasia
Variation info
Gene MEN1
CLNDBN Hereditary cancer-predisposing syndrome Multiple endocrine neoplasia, type 1
Reversed 1
HGVS NC_000011.9:g.64573115G>A; NC_000011.9:g.64573115G>C
CLNSRC
CLNACC RCV000491380.1, RCV000472220.1,