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rs1060500012

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060500012(G;T)
Make rs1060500012(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position193142067
GeneCDC73
is asnp
is mentioned by
dbSNPrs1060500012
dbSNP (old)rs1060500012
ClinGenrs1060500012
ebirs1060500012
HLIrs1060500012
Exacrs1060500012
Gnomadrs1060500012
Varsomers1060500012
Maprs1060500012
PheGenIrs1060500012
Biobankrs1060500012
1000 genomesrs1060500012
hgdprs1060500012
ensemblrs1060500012
gopubmedrs1060500012
geneviewrs1060500012
scholarrs1060500012
googlers1060500012
pharmgkbrs1060500012
gwascentralrs1060500012
openSNPrs1060500012
23andMers1060500012
23andMe allrs1060500012
SNPshotrs1060500012
SNPdbers1060500012
MSV3drs1060500012
GWAS Ctlgrs1060500012
Max Magnitude0
ClinVar
Risk rs1060500012(T;T)
Alt rs1060500012(T;T)
Reference Rs1060500012(G;G)
Significance Probable-Pathogenic
Disease Parathyroid carcinoma
Variation info
Gene CDC73
CLNDBN Parathyroid carcinoma
Reversed 0
HGVS NC_000001.10:g.193111197G>T
CLNSRC
CLNACC RCV000473101.1,