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rs1060500009

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060500009(-;-)
Make rs1060500009(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position193130181
GeneCDC73
is asnp
is mentioned by
dbSNPrs1060500009
dbSNP (old)rs1060500009
ClinGenrs1060500009
ebirs1060500009
HLIrs1060500009
Exacrs1060500009
Gnomadrs1060500009
Varsomers1060500009
Maprs1060500009
PheGenIrs1060500009
Biobankrs1060500009
1000 genomesrs1060500009
hgdprs1060500009
ensemblrs1060500009
gopubmedrs1060500009
geneviewrs1060500009
scholarrs1060500009
googlers1060500009
pharmgkbrs1060500009
gwascentralrs1060500009
openSNPrs1060500009
23andMers1060500009
23andMe allrs1060500009
SNPshotrs1060500009
SNPdbers1060500009
MSV3drs1060500009
GWAS Ctlgrs1060500009
Max Magnitude0
ClinVar
Risk rs1060500009(-;-)
Alt rs1060500009(-;-)
Reference Rs1060500009(A;A)
Significance Pathogenic
Disease Parathyroid carcinoma
Variation info
Gene CDC73 LOC101929160
CLNDBN Parathyroid carcinoma
Reversed 0
HGVS NC_000001.10:g.193099311delA
CLNSRC
CLNACC RCV000458654.1,