rs72558435

Orientation

plus

Stabilized

plus

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

Make rs72558435(C;T)

Make rs72558435(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38408883

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558435
dbSNP (classic)	rs72558435
ClinGen	rs72558435
ebi	rs72558435
HLI	rs72558435
Exac	rs72558435
Gnomad	rs72558435
Varsome	rs72558435
LitVar	rs72558435
Map	rs72558435
PheGenI	rs72558435
Biobank	rs72558435
1000 genomes	rs72558435
hgdp	rs72558435
ensembl	rs72558435
geneview	rs72558435
scholar	rs72558435
google	rs72558435
pharmgkb	rs72558435
gwascentral	rs72558435
openSNP	rs72558435
23andMe	rs72558435
SNPshot	rs72558435
SNPdbe	rs72558435
MSV3d	rs72558435
GWAS Ctlg	rs72558435

Max Magnitude

0

ClinVar
Risk	rs72558435(A;A) rs72558435(T;T)
Alt	rs72558435(A;A) rs72558435(T;T)
Reference	Rs72558435(C;C)
Significance	Pathogenic
Disease	not specified not provided
Variation	info
Gene	OTC
CLNDBN	not specified not provided
Reversed	0
HGVS	NC_000023.10:g.38268136C>A; NC_000023.10:g.38268136C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000153627.3, RCV000083551.1,