rs281865554

Orientation

plus

Stabilized

plus

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

Make rs281865554(C;C)

Make rs281865554(C;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38367290

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs281865554
dbSNP (classic)	rs281865554
ClinGen	rs281865554
ebi	rs281865554
HLI	rs281865554
Exac	rs281865554
Gnomad	rs281865554
Varsome	rs281865554
LitVar	rs281865554
Map	rs281865554
PheGenI	rs281865554
Biobank	rs281865554
1000 genomes	rs281865554
hgdp	rs281865554
ensembl	rs281865554
geneview	rs281865554
scholar	rs281865554
google	rs281865554
pharmgkb	rs281865554
gwascentral	rs281865554
openSNP	rs281865554
23andMe	rs281865554
SNPshot	rs281865554
SNPdbe	rs281865554
MSV3d	rs281865554
GWAS Ctlg	rs281865554

Max Magnitude

0

ClinVar
Risk	rs281865554(C;C)
Alt	rs281865554(C;C)
Reference	Rs281865554(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38226543G>C
CLNSRC	ClinVar
CLNACC	RCV000083567.1,