rs72554305

Orientation

plus

Stabilized

plus

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

Make rs72554305(C;T)

Make rs72554305(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38367319

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72554305
dbSNP (classic)	rs72554305
ClinGen	rs72554305
ebi	rs72554305
HLI	rs72554305
Exac	rs72554305
Gnomad	rs72554305
Varsome	rs72554305
LitVar	rs72554305
Map	rs72554305
PheGenI	rs72554305
Biobank	rs72554305
1000 genomes	rs72554305
hgdp	rs72554305
ensembl	rs72554305
geneview	rs72554305
scholar	rs72554305
google	rs72554305
pharmgkb	rs72554305
gwascentral	rs72554305
openSNP	rs72554305
23andMe	rs72554305
SNPshot	rs72554305
SNPdbe	rs72554305
MSV3d	rs72554305
GWAS Ctlg	rs72554305

Max Magnitude

0

ClinVar
Risk	rs72554305(G;G) rs72554305(T;T)
Alt	rs72554305(G;G) rs72554305(T;T)
Reference	Rs72554305(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38226572C>T
CLNSRC	ClinVar
CLNACC	RCV000083330.1,