rs72556259

Orientation

plus

Stabilized

plus

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

Make rs72556259(C;C)

Make rs72556259(C;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38401304

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556259
dbSNP (classic)	rs72556259
ClinGen	rs72556259
ebi	rs72556259
HLI	rs72556259
Exac	rs72556259
Gnomad	rs72556259
Varsome	rs72556259
LitVar	rs72556259
Map	rs72556259
PheGenI	rs72556259
Biobank	rs72556259
1000 genomes	rs72556259
hgdp	rs72556259
ensembl	rs72556259
geneview	rs72556259
scholar	rs72556259
google	rs72556259
pharmgkb	rs72556259
gwascentral	rs72556259
openSNP	rs72556259
23andMe	rs72556259
SNPshot	rs72556259
SNPdbe	rs72556259
MSV3d	rs72556259
GWAS Ctlg	rs72556259

Max Magnitude

0

ClinVar
Risk	rs72556259(C;C)
Alt	rs72556259(C;C)
Reference	Rs72556259(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38260557T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000083430.1,