rs72554349

Orientation

plus

Stabilized

plus

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

Make rs72554349(A;A)

Make rs72554349(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38381342

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72554349
dbSNP (classic)	rs72554349
ClinGen	rs72554349
ebi	rs72554349
HLI	rs72554349
Exac	rs72554349
Gnomad	rs72554349
Varsome	rs72554349
LitVar	rs72554349
Map	rs72554349
PheGenI	rs72554349
Biobank	rs72554349
1000 genomes	rs72554349
hgdp	rs72554349
ensembl	rs72554349
geneview	rs72554349
scholar	rs72554349
google	rs72554349
pharmgkb	rs72554349
gwascentral	rs72554349
openSNP	rs72554349
23andMe	rs72554349
SNPshot	rs72554349
SNPdbe	rs72554349
MSV3d	rs72554349
GWAS Ctlg	rs72554349

Max Magnitude

0

ClinVar
Risk	rs72554349(A;A)
Alt	rs72554349(A;A)
Reference	Rs72554349(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38240595G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000083396.3,