rs72554322

Orientation

plus

Stabilized

plus

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

Make rs72554322(A;A)

Make rs72554322(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38367387

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72554322
dbSNP (classic)	rs72554322
ClinGen	rs72554322
ebi	rs72554322
HLI	rs72554322
Exac	rs72554322
Gnomad	rs72554322
Varsome	rs72554322
LitVar	rs72554322
Map	rs72554322
PheGenI	rs72554322
Biobank	rs72554322
1000 genomes	rs72554322
hgdp	rs72554322
ensembl	rs72554322
geneview	rs72554322
scholar	rs72554322
google	rs72554322
pharmgkb	rs72554322
gwascentral	rs72554322
openSNP	rs72554322
23andMe	rs72554322
SNPshot	rs72554322
SNPdbe	rs72554322
MSV3d	rs72554322
GWAS Ctlg	rs72554322

Max Magnitude

0

ClinVar
Risk	rs72554322(A;A)
Alt	rs72554322(A;A)
Reference	Rs72554322(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38226640G>A
CLNSRC	ClinVar
CLNACC	RCV000083356.1,