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rs1060499992

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499992(G;T)
Make rs1060499992(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position64809764
GeneMEN1
is asnp
is mentioned by
dbSNPrs1060499992
dbSNP (old)rs1060499992
ClinGenrs1060499992
ebirs1060499992
HLIrs1060499992
Exacrs1060499992
Gnomadrs1060499992
Varsomers1060499992
Maprs1060499992
PheGenIrs1060499992
Biobankrs1060499992
1000 genomesrs1060499992
hgdprs1060499992
ensemblrs1060499992
gopubmedrs1060499992
geneviewrs1060499992
scholarrs1060499992
googlers1060499992
pharmgkbrs1060499992
gwascentralrs1060499992
openSNPrs1060499992
23andMers1060499992
23andMe allrs1060499992
SNPshotrs1060499992
SNPdbers1060499992
MSV3drs1060499992
GWAS Ctlgrs1060499992
Max Magnitude0
ClinVar
Risk rs1060499992(T;T)
Alt rs1060499992(T;T)
Reference Rs1060499992(G;G)
Significance Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene MEN1
CLNDBN Multiple endocrine neoplasia, type 1
Reversed 1
HGVS NC_000011.9:g.64577236C>A
CLNSRC
CLNACC RCV000469372.1,