rs72558478

Orientation

plus

Stabilized

plus

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

Make rs72558478(A;G)

Make rs72558478(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38411982

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558478
dbSNP (classic)	rs72558478
ClinGen	rs72558478
ebi	rs72558478
HLI	rs72558478
Exac	rs72558478
Gnomad	rs72558478
Varsome	rs72558478
LitVar	rs72558478
Map	rs72558478
PheGenI	rs72558478
Biobank	rs72558478
1000 genomes	rs72558478
hgdp	rs72558478
ensembl	rs72558478
geneview	rs72558478
scholar	rs72558478
google	rs72558478
pharmgkb	rs72558478
gwascentral	rs72558478
openSNP	rs72558478
23andMe	rs72558478
SNPshot	rs72558478
SNPdbe	rs72558478
MSV3d	rs72558478
GWAS Ctlg	rs72558478

Max Magnitude

0

ClinVar
Risk	rs72558478(G;G)
Alt	rs72558478(G;G)
Reference	Rs72558478(A;A)
Significance	Other
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38271235A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000083625.1,