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rs1064793169

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome11
Position64806359
GeneMEN1
is asnp
is mentioned by
dbSNPrs1064793169
dbSNP (old)rs1064793169
ClinGenrs1064793169
ebirs1064793169
HLIrs1064793169
Exacrs1064793169
Gnomadrs1064793169
Varsomers1064793169
Maprs1064793169
PheGenIrs1064793169
Biobankrs1064793169
1000 genomesrs1064793169
hgdprs1064793169
ensemblrs1064793169
gopubmedrs1064793169
geneviewrs1064793169
scholarrs1064793169
googlers1064793169
pharmgkbrs1064793169
gwascentralrs1064793169
openSNPrs1064793169
23andMers1064793169
23andMe allrs1064793169
SNPshotrs1064793169
SNPdbers1064793169
MSV3drs1064793169
GWAS Ctlgrs1064793169
Max Magnitude0
ClinVar
Risk rs1064793169(C;C)
Alt rs1064793169(C;C)
Reference Rs1064793169(T;T)
Significance Probable-Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene MEN1
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000011.9:g.64573831A>G
CLNSRC
CLNACC RCV000482667.1, RCV000491064.1,