rs72558479

Orientation

plus

Stabilized

plus

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

Make rs72558479(A;T)

Make rs72558479(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38411985

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558479
dbSNP (classic)	rs72558479
ClinGen	rs72558479
ebi	rs72558479
HLI	rs72558479
Exac	rs72558479
Gnomad	rs72558479
Varsome	rs72558479
LitVar	rs72558479
Map	rs72558479
PheGenI	rs72558479
Biobank	rs72558479
1000 genomes	rs72558479
hgdp	rs72558479
ensembl	rs72558479
geneview	rs72558479
scholar	rs72558479
google	rs72558479
pharmgkb	rs72558479
gwascentral	rs72558479
openSNP	rs72558479
23andMe	rs72558479
SNPshot	rs72558479
SNPdbe	rs72558479
MSV3d	rs72558479
GWAS Ctlg	rs72558479

Max Magnitude

0

ClinVar
Risk	rs72558479(T;T)
Alt	rs72558479(T;T)
Reference	Rs72558479(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38271238A>T
CLNSRC	ClinVar
CLNACC	RCV000083626.1,