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rs1057521110

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521110(A;A)
Make rs1057521110(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position64807662
GeneMEN1
is asnp
is mentioned by
dbSNPrs1057521110
dbSNP (old)rs1057521110
ClinGenrs1057521110
ebirs1057521110
HLIrs1057521110
Exacrs1057521110
Gnomadrs1057521110
Varsomers1057521110
Maprs1057521110
PheGenIrs1057521110
Biobankrs1057521110
1000 genomesrs1057521110
hgdprs1057521110
ensemblrs1057521110
gopubmedrs1057521110
geneviewrs1057521110
scholarrs1057521110
googlers1057521110
pharmgkbrs1057521110
gwascentralrs1057521110
openSNPrs1057521110
23andMers1057521110
23andMe allrs1057521110
SNPshotrs1057521110
SNPdbers1057521110
MSV3drs1057521110
GWAS Ctlgrs1057521110
Max Magnitude0
ClinVar
Risk rs1057521110(A;A)
Alt rs1057521110(A;A)
Reference Rs1057521110(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64575134C>T
CLNSRC
CLNACC RCV000433003.1,