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rs1060499990

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499990(-;-)
Make rs1060499990(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position64809942
GeneMEN1
is asnp
is mentioned by
dbSNPrs1060499990
dbSNP (old)rs1060499990
ClinGenrs1060499990
ebirs1060499990
HLIrs1060499990
Exacrs1060499990
Gnomadrs1060499990
Varsomers1060499990
Maprs1060499990
PheGenIrs1060499990
Biobankrs1060499990
1000 genomesrs1060499990
hgdprs1060499990
ensemblrs1060499990
gopubmedrs1060499990
geneviewrs1060499990
scholarrs1060499990
googlers1060499990
pharmgkbrs1060499990
gwascentralrs1060499990
openSNPrs1060499990
23andMers1060499990
23andMe allrs1060499990
SNPshotrs1060499990
SNPdbers1060499990
MSV3drs1060499990
GWAS Ctlgrs1060499990
Max Magnitude0
ClinVar
Risk rs1060499990(-;-)
Alt rs1060499990(-;-)
Reference Rs1060499990(C;C)
Significance Pathogenic
Disease Multiple endocrine neoplasia not provided
Variation info
Gene MEN1
CLNDBN Multiple endocrine neoplasia, type 1 not provided
Reversed 1
HGVS NC_000011.9:g.64577414delG
CLNSRC
CLNACC RCV000460562.1, RCV000486690.1,