rs72552301

Orientation

plus

Stabilized

plus

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

Make rs72552301(A;C)

Make rs72552301(C;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38352777

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72552301
dbSNP (classic)	rs72552301
ClinGen	rs72552301
ebi	rs72552301
HLI	rs72552301
Exac	rs72552301
Gnomad	rs72552301
Varsome	rs72552301
LitVar	rs72552301
Map	rs72552301
PheGenI	rs72552301
Biobank	rs72552301
1000 genomes	rs72552301
hgdp	rs72552301
ensembl	rs72552301
geneview	rs72552301
scholar	rs72552301
google	rs72552301
pharmgkb	rs72552301
gwascentral	rs72552301
openSNP	rs72552301
23andMe	rs72552301
SNPshot	rs72552301
SNPdbe	rs72552301
MSV3d	rs72552301
GWAS Ctlg	rs72552301

Max Magnitude

0

ClinVar
Risk	rs72552301(C;C)
Alt	rs72552301(C;C)
Reference	Rs72552301(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38212030A>C
CLNSRC	ClinVar
CLNACC	RCV000083562.1,