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rs1057517902

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517902(-;-)
Make rs1057517902(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position64809903
GeneMEN1
is asnp
is mentioned by
dbSNPrs1057517902
dbSNP (old)rs1057517902
ClinGenrs1057517902
ebirs1057517902
HLIrs1057517902
Exacrs1057517902
Gnomadrs1057517902
Varsomers1057517902
Maprs1057517902
PheGenIrs1057517902
Biobankrs1057517902
1000 genomesrs1057517902
hgdprs1057517902
ensemblrs1057517902
gopubmedrs1057517902
geneviewrs1057517902
scholarrs1057517902
googlers1057517902
pharmgkbrs1057517902
gwascentralrs1057517902
openSNPrs1057517902
23andMers1057517902
23andMe allrs1057517902
SNPshotrs1057517902
SNPdbers1057517902
MSV3drs1057517902
GWAS Ctlgrs1057517902
Max Magnitude0
ClinVar
Risk rs1057517902(-;-)
Alt rs1057517902(-;-)
Reference Rs1057517902(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64577375delG
CLNSRC
CLNACC RCV000412904.1,