rs281865552

Orientation

plus

Stabilized

plus

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

Make rs281865552(C;C)

Make rs281865552(C;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38403740

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs281865552
dbSNP (classic)	rs281865552
ClinGen	rs281865552
ebi	rs281865552
HLI	rs281865552
Exac	rs281865552
Gnomad	rs281865552
Varsome	rs281865552
LitVar	rs281865552
Map	rs281865552
PheGenI	rs281865552
Biobank	rs281865552
1000 genomes	rs281865552
hgdp	rs281865552
ensembl	rs281865552
geneview	rs281865552
scholar	rs281865552
google	rs281865552
pharmgkb	rs281865552
gwascentral	rs281865552
openSNP	rs281865552
23andMe	rs281865552
SNPshot	rs281865552
SNPdbe	rs281865552
MSV3d	rs281865552
GWAS Ctlg	rs281865552

Max Magnitude

0

ClinVar
Risk	rs281865552(A;A) rs281865552(C;C)
Alt	rs281865552(A;A) rs281865552(C;C)
Reference	Rs281865552(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38262993G>A; NC_000023.10:g.38262993G>C
CLNSRC	ClinVar
CLNACC	RCV000083530.1, RCV000083531.1,