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rs1057518572

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518572(A;A)
Make rs1057518572(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position64806369
GeneMEN1
is asnp
is mentioned by
dbSNPrs1057518572
dbSNP (old)rs1057518572
ClinGenrs1057518572
ebirs1057518572
HLIrs1057518572
Exacrs1057518572
Gnomadrs1057518572
Varsomers1057518572
Maprs1057518572
PheGenIrs1057518572
Biobankrs1057518572
1000 genomesrs1057518572
hgdprs1057518572
ensemblrs1057518572
gopubmedrs1057518572
geneviewrs1057518572
scholarrs1057518572
googlers1057518572
pharmgkbrs1057518572
gwascentralrs1057518572
openSNPrs1057518572
23andMers1057518572
23andMe allrs1057518572
SNPshotrs1057518572
SNPdbers1057518572
MSV3drs1057518572
GWAS Ctlgrs1057518572
Max Magnitude0
ClinVar
Risk rs1057518572(A;A)
Alt rs1057518572(A;A)
Reference Rs1057518572(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64573841C>T
CLNSRC
CLNACC RCV000414731.1,