rs72554317

Orientation

plus

Stabilized

plus

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

Make rs72554317(A;G)

Make rs72554317(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38367368

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72554317
dbSNP (classic)	rs72554317
ClinGen	rs72554317
ebi	rs72554317
HLI	rs72554317
Exac	rs72554317
Gnomad	rs72554317
Varsome	rs72554317
LitVar	rs72554317
Map	rs72554317
PheGenI	rs72554317
Biobank	rs72554317
1000 genomes	rs72554317
hgdp	rs72554317
ensembl	rs72554317
geneview	rs72554317
scholar	rs72554317
google	rs72554317
pharmgkb	rs72554317
gwascentral	rs72554317
openSNP	rs72554317
23andMe	rs72554317
SNPshot	rs72554317
SNPdbe	rs72554317
MSV3d	rs72554317
GWAS Ctlg	rs72554317

Max Magnitude

0

ClinVar
Risk	rs72554317(G;G)
Alt	rs72554317(G;G)
Reference	Rs72554317(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38226621A>G
CLNSRC	ClinVar
CLNACC	RCV000083349.1,