rs72558418

Orientation

plus

Stabilized

plus

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

Make rs72558418(A;C)

Make rs72558418(C;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38403705

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72558418
dbSNP (classic)	rs72558418
ClinGen	rs72558418
ebi	rs72558418
HLI	rs72558418
Exac	rs72558418
Gnomad	rs72558418
Varsome	rs72558418
LitVar	rs72558418
Map	rs72558418
PheGenI	rs72558418
Biobank	rs72558418
1000 genomes	rs72558418
hgdp	rs72558418
ensembl	rs72558418
geneview	rs72558418
scholar	rs72558418
google	rs72558418
pharmgkb	rs72558418
gwascentral	rs72558418
openSNP	rs72558418
23andMe	rs72558418
SNPshot	rs72558418
SNPdbe	rs72558418
MSV3d	rs72558418
GWAS Ctlg	rs72558418

Max Magnitude

0

ClinVar
Risk	rs72558418(C;C)
Alt	rs72558418(C;C)
Reference	Rs72558418(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38262958A>C
CLNSRC	ClinVar
CLNACC	RCV000083519.1,