rs72556279

Orientation

plus

Stabilized

plus

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

Make rs72556279(A;T)

Make rs72556279(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38401402

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556279
dbSNP (classic)	rs72556279
ClinGen	rs72556279
ebi	rs72556279
HLI	rs72556279
Exac	rs72556279
Gnomad	rs72556279
Varsome	rs72556279
LitVar	rs72556279
Map	rs72556279
PheGenI	rs72556279
Biobank	rs72556279
1000 genomes	rs72556279
hgdp	rs72556279
ensembl	rs72556279
geneview	rs72556279
scholar	rs72556279
google	rs72556279
pharmgkb	rs72556279
gwascentral	rs72556279
openSNP	rs72556279
23andMe	rs72556279
SNPshot	rs72556279
SNPdbe	rs72556279
MSV3d	rs72556279
GWAS Ctlg	rs72556279

Max Magnitude

0

ClinVar
Risk	rs72556279(T;T)
Alt	rs72556279(T;T)
Reference	Rs72556279(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38260655A>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000083469.1,