rs72556270

Orientation

plus

Stabilized

plus

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

Make rs72556270(A;G)

Make rs72556270(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38401369

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556270
dbSNP (classic)	rs72556270
ClinGen	rs72556270
ebi	rs72556270
HLI	rs72556270
Exac	rs72556270
Gnomad	rs72556270
Varsome	rs72556270
LitVar	rs72556270
Map	rs72556270
PheGenI	rs72556270
Biobank	rs72556270
1000 genomes	rs72556270
hgdp	rs72556270
ensembl	rs72556270
geneview	rs72556270
scholar	rs72556270
google	rs72556270
pharmgkb	rs72556270
gwascentral	rs72556270
openSNP	rs72556270
23andMe	rs72556270
SNPshot	rs72556270
SNPdbe	rs72556270
MSV3d	rs72556270
GWAS Ctlg	rs72556270

Max Magnitude

0

ClinVar
Risk	rs72556270(G;G)
Alt	rs72556270(G;G)
Reference	Rs72556270(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38260622A>G
CLNSRC	ClinVar
CLNACC	RCV000083454.1,