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rs1060500019

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs1060500019(-;-)
Make rs1060500019(-;GA)
Make rs1060500019(GA;GA)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position193138116
GeneCDC73
is asnp
is mentioned by
dbSNPrs1060500019
dbSNP (old)rs1060500019
ClinGenrs1060500019
ebirs1060500019
HLIrs1060500019
Exacrs1060500019
Gnomadrs1060500019
Varsomers1060500019
Maprs1060500019
PheGenIrs1060500019
Biobankrs1060500019
1000 genomesrs1060500019
hgdprs1060500019
ensemblrs1060500019
gopubmedrs1060500019
geneviewrs1060500019
scholarrs1060500019
googlers1060500019
pharmgkbrs1060500019
gwascentralrs1060500019
openSNPrs1060500019
23andMers1060500019
23andMe allrs1060500019
SNPshotrs1060500019
SNPdbers1060500019
MSV3drs1060500019
GWAS Ctlgrs1060500019
Max Magnitude0
ClinVar
Risk rs1060500019(-;-)
Alt rs1060500019(-;-)
Reference Rs1060500019(AG;AG)
Significance Pathogenic
Disease Parathyroid carcinoma
Variation info
Gene CDC73
CLNDBN Parathyroid carcinoma
Reversed 0
HGVS NC_000001.10:g.193107246_193107247delGA
CLNSRC
CLNACC RCV000477581.1,