rs121434263

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs121434263(A;A)

Make rs121434263(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

193122328

Gene	CDC73, LOC101929160

is a	snp
is	mentioned by
dbSNP	rs121434263
dbSNP (classic)	rs121434263
ClinGen	rs121434263
ebi	rs121434263
HLI	rs121434263
Exac	rs121434263
Gnomad	rs121434263
Varsome	rs121434263
LitVar	rs121434263
Map	rs121434263
PheGenI	rs121434263
Biobank	rs121434263
1000 genomes	rs121434263
hgdp	rs121434263
ensembl	rs121434263
geneview	rs121434263
scholar	rs121434263
google	rs121434263
pharmgkb	rs121434263
gwascentral	rs121434263
openSNP	rs121434263
23andMe	rs121434263
SNPshot	rs121434263
SNPdbe	rs121434263
MSV3d	rs121434263
GWAS Ctlg	rs121434263

Max Magnitude

0

OMIM	607393
Desc
Variant	0005
Related	also

ClinVar
Risk	rs121434263(A;A)
Alt	rs121434263(A;A)
Reference	Rs121434263(G;G)
Significance	Pathogenic
Disease	Parathyroid carcinoma
Variation	info
Gene	CDC73 LOC101929160
CLNDBN	Parathyroid carcinoma
Reversed	0
HGVS	NC_000001.10:g.193091458G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003430.4,