rs72558433

Orientation

plus

Stabilized

plus

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

Make rs72558433(A;G)

Make rs72558433(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38408874

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558433
dbSNP (classic)	rs72558433
ClinGen	rs72558433
ebi	rs72558433
HLI	rs72558433
Exac	rs72558433
Gnomad	rs72558433
Varsome	rs72558433
LitVar	rs72558433
Map	rs72558433
PheGenI	rs72558433
Biobank	rs72558433
1000 genomes	rs72558433
hgdp	rs72558433
ensembl	rs72558433
geneview	rs72558433
scholar	rs72558433
google	rs72558433
pharmgkb	rs72558433
gwascentral	rs72558433
openSNP	rs72558433
23andMe	rs72558433
SNPshot	rs72558433
SNPdbe	rs72558433
MSV3d	rs72558433
GWAS Ctlg	rs72558433

Max Magnitude

0

ClinVar
Risk	rs72558433(G;G)
Alt	rs72558433(G;G)
Reference	Rs72558433(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38268127A>G
CLNSRC	ClinVar
CLNACC	RCV000083549.1,