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rs1064793398

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome11
Position64807174
GeneMEN1
is asnp
is mentioned by
dbSNPrs1064793398
dbSNP (old)rs1064793398
ClinGenrs1064793398
ebirs1064793398
HLIrs1064793398
Exacrs1064793398
Gnomadrs1064793398
Varsomers1064793398
Maprs1064793398
PheGenIrs1064793398
Biobankrs1064793398
1000 genomesrs1064793398
hgdprs1064793398
ensemblrs1064793398
gopubmedrs1064793398
geneviewrs1064793398
scholarrs1064793398
googlers1064793398
pharmgkbrs1064793398
gwascentralrs1064793398
openSNPrs1064793398
23andMers1064793398
23andMe allrs1064793398
SNPshotrs1064793398
SNPdbers1064793398
MSV3drs1064793398
GWAS Ctlgrs1064793398
Max Magnitude0
ClinVar
Risk rs1064793398(A;A)
Alt rs1064793398(A;A)
Reference Rs1064793398(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64574646C>T
CLNSRC
CLNACC RCV000484677.1,