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rs1060500020

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060500020(-;-)
Make rs1060500020(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position193122204
GeneCDC73, LOC101929160
is asnp
is mentioned by
dbSNPrs1060500020
dbSNP (old)rs1060500020
ClinGenrs1060500020
ebirs1060500020
HLIrs1060500020
Exacrs1060500020
Gnomadrs1060500020
Varsomers1060500020
Maprs1060500020
PheGenIrs1060500020
Biobankrs1060500020
1000 genomesrs1060500020
hgdprs1060500020
ensemblrs1060500020
gopubmedrs1060500020
geneviewrs1060500020
scholarrs1060500020
googlers1060500020
pharmgkbrs1060500020
gwascentralrs1060500020
openSNPrs1060500020
23andMers1060500020
23andMe allrs1060500020
SNPshotrs1060500020
SNPdbers1060500020
MSV3drs1060500020
GWAS Ctlgrs1060500020
Max Magnitude0
ClinVar
Risk rs1060500020(-;-)
Alt rs1060500020(-;-)
Reference Rs1060500020(G;G)
Significance Pathogenic
Disease Parathyroid carcinoma
Variation info
Gene CDC73 LOC101929160
CLNDBN Parathyroid carcinoma
Reversed 0
HGVS NC_000001.10:g.193091334delG
CLNSRC
CLNACC RCV000463923.1,