rs72558486

Orientation

plus

Stabilized

plus

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

Make rs72558486(G;T)

Make rs72558486(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38421023

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558486
dbSNP (classic)	rs72558486
ClinGen	rs72558486
ebi	rs72558486
HLI	rs72558486
Exac	rs72558486
Gnomad	rs72558486
Varsome	rs72558486
LitVar	rs72558486
Map	rs72558486
PheGenI	rs72558486
Biobank	rs72558486
1000 genomes	rs72558486
hgdp	rs72558486
ensembl	rs72558486
geneview	rs72558486
scholar	rs72558486
google	rs72558486
pharmgkb	rs72558486
gwascentral	rs72558486
openSNP	rs72558486
23andMe	rs72558486
SNPshot	rs72558486
SNPdbe	rs72558486
MSV3d	rs72558486
GWAS Ctlg	rs72558486

Max Magnitude

0

ClinVar
Risk	rs72558486(T;T)
Alt	rs72558486(T;T)
Reference	Rs72558486(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38280276G>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000083318.1,