rs72554330

Orientation

plus

Stabilized

plus

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

Make rs72554330(C;T)

Make rs72554330(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38369811

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72554330
dbSNP (classic)	rs72554330
ClinGen	rs72554330
ebi	rs72554330
HLI	rs72554330
Exac	rs72554330
Gnomad	rs72554330
Varsome	rs72554330
LitVar	rs72554330
Map	rs72554330
PheGenI	rs72554330
Biobank	rs72554330
1000 genomes	rs72554330
hgdp	rs72554330
ensembl	rs72554330
geneview	rs72554330
scholar	rs72554330
google	rs72554330
pharmgkb	rs72554330
gwascentral	rs72554330
openSNP	rs72554330
23andMe	rs72554330
SNPshot	rs72554330
SNPdbe	rs72554330
MSV3d	rs72554330
GWAS Ctlg	rs72554330

Max Magnitude

0

ClinVar
Risk	rs72554330(T;T)
Alt	rs72554330(T;T)
Reference	Rs72554330(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38229064C>T
CLNSRC	ClinVar
CLNACC	RCV000083368.1,