rs72558421

Orientation

plus

Stabilized

plus

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

Make rs72558421(C;T)

Make rs72558421(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38403720

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558421
dbSNP (classic)	rs72558421
ClinGen	rs72558421
ebi	rs72558421
HLI	rs72558421
Exac	rs72558421
Gnomad	rs72558421
Varsome	rs72558421
LitVar	rs72558421
Map	rs72558421
PheGenI	rs72558421
Biobank	rs72558421
1000 genomes	rs72558421
hgdp	rs72558421
ensembl	rs72558421
geneview	rs72558421
scholar	rs72558421
google	rs72558421
pharmgkb	rs72558421
gwascentral	rs72558421
openSNP	rs72558421
23andMe	rs72558421
SNPshot	rs72558421
SNPdbe	rs72558421
MSV3d	rs72558421
GWAS Ctlg	rs72558421

Max Magnitude

0

ClinVar
Risk	rs72558421(T;T)
Alt	rs72558421(T;T)
Reference	Rs72558421(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38262973C>T
CLNSRC	ClinVar
CLNACC	RCV000083521.1,