rs72558424

Orientation

plus

Stabilized

plus

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

Make rs72558424(A;A)

Make rs72558424(A;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38403727

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558424
dbSNP (classic)	rs72558424
ClinGen	rs72558424
ebi	rs72558424
HLI	rs72558424
Exac	rs72558424
Gnomad	rs72558424
Varsome	rs72558424
LitVar	rs72558424
Map	rs72558424
PheGenI	rs72558424
Biobank	rs72558424
1000 genomes	rs72558424
hgdp	rs72558424
ensembl	rs72558424
geneview	rs72558424
scholar	rs72558424
google	rs72558424
pharmgkb	rs72558424
gwascentral	rs72558424
openSNP	rs72558424
23andMe	rs72558424
SNPshot	rs72558424
SNPdbe	rs72558424
MSV3d	rs72558424
GWAS Ctlg	rs72558424

Max Magnitude

0

ClinVar
Risk	rs72558424(A;A)
Alt	rs72558424(A;A)
Reference	Rs72558424(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38262980C>A
CLNSRC	ClinVar
CLNACC	RCV000083524.1,