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rs1060499974

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499974(C;T)
Make rs1060499974(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position64805141
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs1060499974
dbSNP (old)rs1060499974
ClinGenrs1060499974
ebirs1060499974
HLIrs1060499974
Exacrs1060499974
Gnomadrs1060499974
Varsomers1060499974
Maprs1060499974
PheGenIrs1060499974
Biobankrs1060499974
1000 genomesrs1060499974
hgdprs1060499974
ensemblrs1060499974
gopubmedrs1060499974
geneviewrs1060499974
scholarrs1060499974
googlers1060499974
pharmgkbrs1060499974
gwascentralrs1060499974
openSNPrs1060499974
23andMers1060499974
23andMe allrs1060499974
SNPshotrs1060499974
SNPdbers1060499974
MSV3drs1060499974
GWAS Ctlgrs1060499974
Max Magnitude0
ClinVar
Risk rs1060499974(T;T)
Alt rs1060499974(T;T)
Reference Rs1060499974(C;C)
Significance Pathogenic
Disease Multiple endocrine neoplasia not provided Hereditary cancer-predisposing syndrome
Variation info
Gene MAP4K2 MEN1
CLNDBN Multiple endocrine neoplasia, type 1 not provided Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000011.9:g.64572613G>A
CLNSRC
CLNACC RCV000456454.1, RCV000486722.1, RCV000491295.1,