rs72554303

Orientation

plus

Stabilized

plus

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

Make rs72554303(C;G)

Make rs72554303(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38367288

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72554303
dbSNP (classic)	rs72554303
ClinGen	rs72554303
ebi	rs72554303
HLI	rs72554303
Exac	rs72554303
Gnomad	rs72554303
Varsome	rs72554303
LitVar	rs72554303
Map	rs72554303
PheGenI	rs72554303
Biobank	rs72554303
1000 genomes	rs72554303
hgdp	rs72554303
ensembl	rs72554303
geneview	rs72554303
scholar	rs72554303
google	rs72554303
pharmgkb	rs72554303
gwascentral	rs72554303
openSNP	rs72554303
23andMe	rs72554303
SNPshot	rs72554303
SNPdbe	rs72554303
MSV3d	rs72554303
GWAS Ctlg	rs72554303

Max Magnitude

0

ClinVar
Risk	rs72554303(G;G)
Alt	rs72554303(G;G)
Reference	Rs72554303(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38226541C>G
CLNSRC	ClinVar
CLNACC	RCV000083568.1,