rs72558491

Orientation

plus

Stabilized

plus

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

Make rs72558491(A;A)

Make rs72558491(A;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38421045

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558491
dbSNP (classic)	rs72558491
ClinGen	rs72558491
ebi	rs72558491
HLI	rs72558491
Exac	rs72558491
Gnomad	rs72558491
Varsome	rs72558491
LitVar	rs72558491
Map	rs72558491
PheGenI	rs72558491
Biobank	rs72558491
1000 genomes	rs72558491
hgdp	rs72558491
ensembl	rs72558491
geneview	rs72558491
scholar	rs72558491
google	rs72558491
pharmgkb	rs72558491
gwascentral	rs72558491
openSNP	rs72558491
23andMe	rs72558491
SNPshot	rs72558491
SNPdbe	rs72558491
MSV3d	rs72558491
GWAS Ctlg	rs72558491

Max Magnitude

0

ClinVar
Risk	rs72558491(A;A)
Alt	rs72558491(A;A)
Reference	Rs72558491(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38280298C>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000083323.1,