rs587776560

Orientation

plus

Stabilized

plus

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

Make rs587776560(-;-)

Make rs587776560(-;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

193122285

Gene	CDC73, LOC101929160

is a	snp
is	mentioned by
dbSNP	rs587776560
dbSNP (classic)	rs587776560
ClinGen	rs587776560
ebi	rs587776560
HLI	rs587776560
Exac	rs587776560
Gnomad	rs587776560
Varsome	rs587776560
LitVar	rs587776560
Map	rs587776560
PheGenI	rs587776560
Biobank	rs587776560
1000 genomes	rs587776560
hgdp	rs587776560
ensembl	rs587776560
geneview	rs587776560
scholar	rs587776560
google	rs587776560
pharmgkb	rs587776560
gwascentral	rs587776560
openSNP	rs587776560
23andMe	rs587776560
SNPshot	rs587776560
SNPdbe	rs587776560
MSV3d	rs587776560
GWAS Ctlg	rs587776560

Max Magnitude

0

ClinVar
Risk	rs587776560(-;-)
Alt	rs587776560(-;-)
Reference	Rs587776560(G;G)
Significance	Pathogenic
Disease	Parathyroid carcinoma
Variation	info
Gene	CDC73 LOC101929160
CLNDBN	Parathyroid carcinoma
Reversed	0
HGVS	NC_000001.10:g.193091415delG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003441.5,