rs1060500020

Orientation

plus

Stabilized

plus

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

Make rs1060500020(-;-)

Make rs1060500020(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

193122204

Gene	CDC73, LOC101929160

is a	snp
is	mentioned by
dbSNP	rs1060500020
dbSNP (classic)	rs1060500020
ClinGen	rs1060500020
ebi	rs1060500020
HLI	rs1060500020
Exac	rs1060500020
Gnomad	rs1060500020
Varsome	rs1060500020
LitVar	rs1060500020
Map	rs1060500020
PheGenI	rs1060500020
Biobank	rs1060500020
1000 genomes	rs1060500020
hgdp	rs1060500020
ensembl	rs1060500020
geneview	rs1060500020
scholar	rs1060500020
google	rs1060500020
pharmgkb	rs1060500020
gwascentral	rs1060500020
openSNP	rs1060500020
23andMe	rs1060500020
SNPshot	rs1060500020
SNPdbe	rs1060500020
MSV3d	rs1060500020
GWAS Ctlg	rs1060500020

Max Magnitude

0

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,