rs72556286

Orientation

plus

Stabilized

plus

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

Make rs72556286(C;C)

Make rs72556286(C;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38401424

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556286
dbSNP (classic)	rs72556286
ClinGen	rs72556286
ebi	rs72556286
HLI	rs72556286
Exac	rs72556286
Gnomad	rs72556286
Varsome	rs72556286
LitVar	rs72556286
Map	rs72556286
PheGenI	rs72556286
Biobank	rs72556286
1000 genomes	rs72556286
hgdp	rs72556286
ensembl	rs72556286
geneview	rs72556286
scholar	rs72556286
google	rs72556286
pharmgkb	rs72556286
gwascentral	rs72556286
openSNP	rs72556286
23andMe	rs72556286
SNPshot	rs72556286
SNPdbe	rs72556286
MSV3d	rs72556286
GWAS Ctlg	rs72556286

Max Magnitude

0

ClinVar
Risk	rs72556286(C;C)
Alt	rs72556286(C;C)
Reference	Rs72556286(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38260677T>C
CLNSRC	ClinVar
CLNACC	RCV000083478.1,