rs72556275

Orientation

plus

Stabilized

plus

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

Make rs72556275(G;T)

Make rs72556275(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38401381

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556275
dbSNP (classic)	rs72556275
ClinGen	rs72556275
ebi	rs72556275
HLI	rs72556275
Exac	rs72556275
Gnomad	rs72556275
Varsome	rs72556275
LitVar	rs72556275
Map	rs72556275
PheGenI	rs72556275
Biobank	rs72556275
1000 genomes	rs72556275
hgdp	rs72556275
ensembl	rs72556275
geneview	rs72556275
scholar	rs72556275
google	rs72556275
pharmgkb	rs72556275
gwascentral	rs72556275
openSNP	rs72556275
23andMe	rs72556275
SNPshot	rs72556275
SNPdbe	rs72556275
MSV3d	rs72556275
GWAS Ctlg	rs72556275

Max Magnitude

0

ClinVar
Risk	rs72556275(T;T)
Alt	rs72556275(T;T)
Reference	Rs72556275(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38260634G>T
CLNSRC	ClinVar
CLNACC	RCV000083461.1,