rs757205958

Orientation

plus

Stabilized

plus

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

Make rs757205958(A;A)

Make rs757205958(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

210605178

Gene

CPS1

is a	snp
is	mentioned by
dbSNP	rs757205958
dbSNP (classic)	rs757205958
ClinGen	rs757205958
ebi	rs757205958
HLI	rs757205958
Exac	rs757205958
Gnomad	rs757205958
Varsome	rs757205958
LitVar	rs757205958
Map	rs757205958
PheGenI	rs757205958
Biobank	rs757205958
1000 genomes	rs757205958
hgdp	rs757205958
ensembl	rs757205958
geneview	rs757205958
scholar	rs757205958
google	rs757205958
pharmgkb	rs757205958
gwascentral	rs757205958
openSNP	rs757205958
23andMe	rs757205958
SNPshot	rs757205958
SNPdbe	rs757205958
MSV3d	rs757205958
GWAS Ctlg	rs757205958

Max Magnitude

0

ClinVar
Risk	rs757205958(A;A) rs757205958(C;C)
Alt	rs757205958(A;A) rs757205958(C;C)
Reference	Rs757205958(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CPS1
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.211469902G>C
CLNSRC
CLNACC	RCV000185818.1,