rs72554318

Orientation

plus

Stabilized

plus

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

Make rs72554318(A;T)

Make rs72554318(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38367369

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72554318
dbSNP (classic)	rs72554318
ClinGen	rs72554318
ebi	rs72554318
HLI	rs72554318
Exac	rs72554318
Gnomad	rs72554318
Varsome	rs72554318
LitVar	rs72554318
Map	rs72554318
PheGenI	rs72554318
Biobank	rs72554318
1000 genomes	rs72554318
hgdp	rs72554318
ensembl	rs72554318
geneview	rs72554318
scholar	rs72554318
google	rs72554318
pharmgkb	rs72554318
gwascentral	rs72554318
openSNP	rs72554318
23andMe	rs72554318
SNPshot	rs72554318
SNPdbe	rs72554318
MSV3d	rs72554318
GWAS Ctlg	rs72554318

Max Magnitude

0

ClinVar
Risk	rs72554318(T;T)
Alt	rs72554318(T;T)
Reference	Rs72554318(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38226622A>T
CLNSRC	ClinVar
CLNACC	RCV000083350.1,