rs281865553

Orientation

plus

Stabilized

plus

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

Make rs281865553(A;A)

Make rs281865553(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38411999

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs281865553
dbSNP (classic)	rs281865553
ClinGen	rs281865553
ebi	rs281865553
HLI	rs281865553
Exac	rs281865553
Gnomad	rs281865553
Varsome	rs281865553
LitVar	rs281865553
Map	rs281865553
PheGenI	rs281865553
Biobank	rs281865553
1000 genomes	rs281865553
hgdp	rs281865553
ensembl	rs281865553
geneview	rs281865553
scholar	rs281865553
google	rs281865553
pharmgkb	rs281865553
gwascentral	rs281865553
openSNP	rs281865553
23andMe	rs281865553
SNPshot	rs281865553
SNPdbe	rs281865553
MSV3d	rs281865553
GWAS Ctlg	rs281865553

Max Magnitude

0

ClinVar
Risk	rs281865553(A;A)
Alt	rs281865553(A;A)
Reference	Rs281865553(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38271252G>A
CLNSRC	ClinVar
CLNACC	RCV000083315.1,