rs72556295

Orientation

plus

Stabilized

plus

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

Make rs72556295(G;T)

Make rs72556295(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38403640

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556295
dbSNP (classic)	rs72556295
ClinGen	rs72556295
ebi	rs72556295
HLI	rs72556295
Exac	rs72556295
Gnomad	rs72556295
Varsome	rs72556295
LitVar	rs72556295
Map	rs72556295
PheGenI	rs72556295
Biobank	rs72556295
1000 genomes	rs72556295
hgdp	rs72556295
ensembl	rs72556295
geneview	rs72556295
scholar	rs72556295
google	rs72556295
pharmgkb	rs72556295
gwascentral	rs72556295
openSNP	rs72556295
23andMe	rs72556295
SNPshot	rs72556295
SNPdbe	rs72556295
MSV3d	rs72556295
GWAS Ctlg	rs72556295

Max Magnitude

0

ClinVar
Risk	rs72556295(T;T)
Alt	rs72556295(T;T)
Reference	Rs72556295(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38262893G>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000083490.1,