rs72558403

Orientation

plus

Stabilized

plus

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

Make rs72558403(A;T)

Make rs72558403(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38403670

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558403
dbSNP (classic)	rs72558403
ClinGen	rs72558403
ebi	rs72558403
HLI	rs72558403
Exac	rs72558403
Gnomad	rs72558403
Varsome	rs72558403
LitVar	rs72558403
Map	rs72558403
PheGenI	rs72558403
Biobank	rs72558403
1000 genomes	rs72558403
hgdp	rs72558403
ensembl	rs72558403
geneview	rs72558403
scholar	rs72558403
google	rs72558403
pharmgkb	rs72558403
gwascentral	rs72558403
openSNP	rs72558403
23andMe	rs72558403
SNPshot	rs72558403
SNPdbe	rs72558403
MSV3d	rs72558403
GWAS Ctlg	rs72558403

Max Magnitude

0

ClinVar
Risk	rs72558403(T;T)
Alt	rs72558403(T;T)
Reference	Rs72558403(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38262923A>T
CLNSRC	ClinVar
CLNACC	RCV000083504.1,