rs72556261

Orientation

plus

Stabilized

plus

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

Make rs72556261(A;A)

Make rs72556261(A;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38401313

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556261
dbSNP (classic)	rs72556261
ClinGen	rs72556261
ebi	rs72556261
HLI	rs72556261
Exac	rs72556261
Gnomad	rs72556261
Varsome	rs72556261
LitVar	rs72556261
Map	rs72556261
PheGenI	rs72556261
Biobank	rs72556261
1000 genomes	rs72556261
hgdp	rs72556261
ensembl	rs72556261
geneview	rs72556261
scholar	rs72556261
google	rs72556261
pharmgkb	rs72556261
gwascentral	rs72556261
openSNP	rs72556261
23andMe	rs72556261
SNPshot	rs72556261
SNPdbe	rs72556261
MSV3d	rs72556261
GWAS Ctlg	rs72556261

Max Magnitude

0

ClinVar
Risk	rs72556261(A;A) rs72556261(G;G)
Alt	rs72556261(A;A) rs72556261(G;G)
Reference	Rs72556261(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38260566T>A
CLNSRC	ClinVar
CLNACC	RCV000083436.1,