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rs1064793167

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome11
Position64808010
GeneMEN1
is asnp
is mentioned by
dbSNPrs1064793167
dbSNP (old)rs1064793167
ClinGenrs1064793167
ebirs1064793167
HLIrs1064793167
Exacrs1064793167
Gnomadrs1064793167
Varsomers1064793167
Maprs1064793167
PheGenIrs1064793167
Biobankrs1064793167
1000 genomesrs1064793167
hgdprs1064793167
ensemblrs1064793167
gopubmedrs1064793167
geneviewrs1064793167
scholarrs1064793167
googlers1064793167
pharmgkbrs1064793167
gwascentralrs1064793167
openSNPrs1064793167
23andMers1064793167
23andMe allrs1064793167
SNPshotrs1064793167
SNPdbers1064793167
MSV3drs1064793167
GWAS Ctlgrs1064793167
Max Magnitude0
ClinVar
Risk rs1064793167(A;A)
Alt rs1064793167(A;A)
Reference Rs1064793167(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64575482C>T
CLNSRC
CLNACC RCV000483982.1,