rs72556254

Orientation

plus

Stabilized

plus

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

Make rs72556254(C;T)

Make rs72556254(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38401283

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556254
dbSNP (classic)	rs72556254
ClinGen	rs72556254
ebi	rs72556254
HLI	rs72556254
Exac	rs72556254
Gnomad	rs72556254
Varsome	rs72556254
LitVar	rs72556254
Map	rs72556254
PheGenI	rs72556254
Biobank	rs72556254
1000 genomes	rs72556254
hgdp	rs72556254
ensembl	rs72556254
geneview	rs72556254
scholar	rs72556254
google	rs72556254
pharmgkb	rs72556254
gwascentral	rs72556254
openSNP	rs72556254
23andMe	rs72556254
SNPshot	rs72556254
SNPdbe	rs72556254
MSV3d	rs72556254
GWAS Ctlg	rs72556254

Max Magnitude

0

ClinVar
Risk	rs72556254(T;T)
Alt	rs72556254(T;T)
Reference	Rs72556254(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38260536C>T
CLNSRC	ClinVar
CLNACC	RCV000083423.1,