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rs1057517760

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057517760(-;AGC)
Make rs1057517760(AGC;AGC)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position64807559
GeneMEN1
is asnp
is mentioned by
dbSNPrs1057517760
dbSNP (old)rs1057517760
ClinGenrs1057517760
ebirs1057517760
HLIrs1057517760
Exacrs1057517760
Gnomadrs1057517760
Varsomers1057517760
LitVarrs1057517760
Maprs1057517760
PheGenIrs1057517760
Biobankrs1057517760
1000 genomesrs1057517760
hgdprs1057517760
ensemblrs1057517760
gopubmedrs1057517760
geneviewrs1057517760
scholarrs1057517760
googlers1057517760
pharmgkbrs1057517760
gwascentralrs1057517760
openSNPrs1057517760
23andMers1057517760
23andMe allrs1057517760
SNPshotrs1057517760
SNPdbers1057517760
MSV3drs1057517760
GWAS Ctlgrs1057517760
Max Magnitude0
ClinVar
Risk rs1057517760(AGC;AGC)
Alt rs1057517760(AGC;AGC)
Reference Rs1057517760(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64575032_64575034dupGCT
CLNSRC
CLNACC RCV000412812.1,