rs72556276

Orientation

plus

Stabilized

plus

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

Make rs72556276(A;A)

Make rs72556276(A;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38401392

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556276
dbSNP (classic)	rs72556276
ClinGen	rs72556276
ebi	rs72556276
HLI	rs72556276
Exac	rs72556276
Gnomad	rs72556276
Varsome	rs72556276
LitVar	rs72556276
Map	rs72556276
PheGenI	rs72556276
Biobank	rs72556276
1000 genomes	rs72556276
hgdp	rs72556276
ensembl	rs72556276
geneview	rs72556276
scholar	rs72556276
google	rs72556276
pharmgkb	rs72556276
gwascentral	rs72556276
openSNP	rs72556276
23andMe	rs72556276
SNPshot	rs72556276
SNPdbe	rs72556276
MSV3d	rs72556276
GWAS Ctlg	rs72556276

Max Magnitude

0

ClinVar
Risk	rs72556276(A;A)
Alt	rs72556276(A;A)
Reference	Rs72556276(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38260645T>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000083466.1,