rs587776558

Orientation

plus

Stabilized

plus

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

Make rs587776558(A;A)

Make rs587776558(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

193122332

Gene	CDC73, LOC101929160

is a	snp
is	mentioned by
dbSNP	rs587776558
dbSNP (classic)	rs587776558
ClinGen	rs587776558
ebi	rs587776558
HLI	rs587776558
Exac	rs587776558
Gnomad	rs587776558
Varsome	rs587776558
LitVar	rs587776558
Map	rs587776558
PheGenI	rs587776558
Biobank	rs587776558
1000 genomes	rs587776558
hgdp	rs587776558
ensembl	rs587776558
geneview	rs587776558
scholar	rs587776558
google	rs587776558
pharmgkb	rs587776558
gwascentral	rs587776558
openSNP	rs587776558
23andMe	rs587776558
SNPshot	rs587776558
SNPdbe	rs587776558
MSV3d	rs587776558
GWAS Ctlg	rs587776558

Max Magnitude

0

ClinVar
Risk	rs587776558(A;A)
Alt	rs587776558(A;A)
Reference	Rs587776558(G;G)
Significance	Pathogenic
Disease	Hyperparathyroidism 1 Parathyroid adenoma not provided
Variation	info
Gene	CDC73 LOC101929160
CLNDBN	Hyperparathyroidism 1 Parathyroid adenoma, somatic not provided
Reversed	0
HGVS	NC_000001.10:g.193091462G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003435.2, RCV000003436.4, RCV000413007.1,