rs72554316

Orientation

plus

Stabilized

plus

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

Make rs72554316(A;C)

Make rs72554316(C;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38367358

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72554316
dbSNP (classic)	rs72554316
ClinGen	rs72554316
ebi	rs72554316
HLI	rs72554316
Exac	rs72554316
Gnomad	rs72554316
Varsome	rs72554316
LitVar	rs72554316
Map	rs72554316
PheGenI	rs72554316
Biobank	rs72554316
1000 genomes	rs72554316
hgdp	rs72554316
ensembl	rs72554316
geneview	rs72554316
scholar	rs72554316
google	rs72554316
pharmgkb	rs72554316
gwascentral	rs72554316
openSNP	rs72554316
23andMe	rs72554316
SNPshot	rs72554316
SNPdbe	rs72554316
MSV3d	rs72554316
GWAS Ctlg	rs72554316

Max Magnitude

0

ClinVar
Risk	rs72554316(C;C)
Alt	rs72554316(C;C)
Reference	Rs72554316(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38226611A>C
CLNSRC	ClinVar
CLNACC	RCV000083344.1,