rs72558416

Orientation

plus

Stabilized

plus

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

Make rs72558416(A;A)

Make rs72558416(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38403699

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558416
dbSNP (classic)	rs72558416
ClinGen	rs72558416
ebi	rs72558416
HLI	rs72558416
Exac	rs72558416
Gnomad	rs72558416
Varsome	rs72558416
LitVar	rs72558416
Map	rs72558416
PheGenI	rs72558416
Biobank	rs72558416
1000 genomes	rs72558416
hgdp	rs72558416
ensembl	rs72558416
geneview	rs72558416
scholar	rs72558416
google	rs72558416
pharmgkb	rs72558416
gwascentral	rs72558416
openSNP	rs72558416
23andMe	rs72558416
SNPshot	rs72558416
SNPdbe	rs72558416
MSV3d	rs72558416
GWAS Ctlg	rs72558416

Max Magnitude

0

ClinVar
Risk	rs72558416(A;A) rs72558416(T;T)
Alt	rs72558416(A;A) rs72558416(T;T)
Reference	Rs72558416(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38262952G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000083517.1,