rs72558481

Orientation

plus

Stabilized

plus

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

Make rs72558481(A;A)

Make rs72558481(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38411989

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558481
dbSNP (classic)	rs72558481
ClinGen	rs72558481
ebi	rs72558481
HLI	rs72558481
Exac	rs72558481
Gnomad	rs72558481
Varsome	rs72558481
LitVar	rs72558481
Map	rs72558481
PheGenI	rs72558481
Biobank	rs72558481
1000 genomes	rs72558481
hgdp	rs72558481
ensembl	rs72558481
geneview	rs72558481
scholar	rs72558481
google	rs72558481
pharmgkb	rs72558481
gwascentral	rs72558481
openSNP	rs72558481
23andMe	rs72558481
SNPshot	rs72558481
SNPdbe	rs72558481
MSV3d	rs72558481
GWAS Ctlg	rs72558481

Max Magnitude

0

ClinVar
Risk	rs72558481(A;A)
Alt	rs72558481(A;A)
Reference	Rs72558481(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38271242G>A
CLNSRC	ClinVar
CLNACC	RCV000083628.1,