rs72556256

Orientation

plus

Stabilized

plus

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

Make rs72556256(A;A)

Make rs72556256(A;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38401292

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556256
dbSNP (classic)	rs72556256
ClinGen	rs72556256
ebi	rs72556256
HLI	rs72556256
Exac	rs72556256
Gnomad	rs72556256
Varsome	rs72556256
LitVar	rs72556256
Map	rs72556256
PheGenI	rs72556256
Biobank	rs72556256
1000 genomes	rs72556256
hgdp	rs72556256
ensembl	rs72556256
geneview	rs72556256
scholar	rs72556256
google	rs72556256
pharmgkb	rs72556256
gwascentral	rs72556256
openSNP	rs72556256
23andMe	rs72556256
SNPshot	rs72556256
SNPdbe	rs72556256
MSV3d	rs72556256
GWAS Ctlg	rs72556256

Max Magnitude

0

ClinVar
Risk	rs72556256(A;A)
Alt	rs72556256(A;A)
Reference	Rs72556256(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38260545C>A
CLNSRC	ClinVar
CLNACC	RCV000083426.1,