rs1060500012

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs1060500012(G;T)

Make rs1060500012(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

193142067

Gene

CDC73

is a	snp
is	mentioned by
dbSNP	rs1060500012
dbSNP (classic)	rs1060500012
ClinGen	rs1060500012
ebi	rs1060500012
HLI	rs1060500012
Exac	rs1060500012
Gnomad	rs1060500012
Varsome	rs1060500012
LitVar	rs1060500012
Map	rs1060500012
PheGenI	rs1060500012
Biobank	rs1060500012
1000 genomes	rs1060500012
hgdp	rs1060500012
ensembl	rs1060500012
geneview	rs1060500012
scholar	rs1060500012
google	rs1060500012
pharmgkb	rs1060500012
gwascentral	rs1060500012
openSNP	rs1060500012
23andMe	rs1060500012
SNPshot	rs1060500012
SNPdbe	rs1060500012
MSV3d	rs1060500012
GWAS Ctlg	rs1060500012

Max Magnitude

0

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,