rs72556281

Orientation

plus

Stabilized

plus

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

Make rs72556281(C;C)

Make rs72556281(C;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38401408

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556281
dbSNP (classic)	rs72556281
ClinGen	rs72556281
ebi	rs72556281
HLI	rs72556281
Exac	rs72556281
Gnomad	rs72556281
Varsome	rs72556281
LitVar	rs72556281
Map	rs72556281
PheGenI	rs72556281
Biobank	rs72556281
1000 genomes	rs72556281
hgdp	rs72556281
ensembl	rs72556281
geneview	rs72556281
scholar	rs72556281
google	rs72556281
pharmgkb	rs72556281
gwascentral	rs72556281
openSNP	rs72556281
23andMe	rs72556281
SNPshot	rs72556281
SNPdbe	rs72556281
MSV3d	rs72556281
GWAS Ctlg	rs72556281

Max Magnitude

0

ClinVar
Risk	rs72556281(A;A) rs72556281(C;C)
Alt	rs72556281(A;A) rs72556281(C;C)
Reference	Rs72556281(G;G)
Significance	Pathogenic
Disease	not specified not provided
Variation	info
Gene	OTC
CLNDBN	not specified not provided
Reversed	0
HGVS	NC_000023.10:g.38260661G>A; NC_000023.10:g.38260661G>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000490084.1, RCV000083471.1,