rs72556288

Orientation

plus

Stabilized

plus

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

Make rs72556288(C;C)

Make rs72556288(C;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38401429

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556288
dbSNP (classic)	rs72556288
ClinGen	rs72556288
ebi	rs72556288
HLI	rs72556288
Exac	rs72556288
Gnomad	rs72556288
Varsome	rs72556288
LitVar	rs72556288
Map	rs72556288
PheGenI	rs72556288
Biobank	rs72556288
1000 genomes	rs72556288
hgdp	rs72556288
ensembl	rs72556288
geneview	rs72556288
scholar	rs72556288
google	rs72556288
pharmgkb	rs72556288
gwascentral	rs72556288
openSNP	rs72556288
23andMe	rs72556288
SNPshot	rs72556288
SNPdbe	rs72556288
MSV3d	rs72556288
GWAS Ctlg	rs72556288

Max Magnitude

0

ClinVar
Risk	rs72556288(C;C)
Alt	rs72556288(C;C)
Reference	Rs72556288(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38260682G>C
CLNSRC	ClinVar
CLNACC	RCV000083480.1,