rs72556252

Orientation

plus

Stabilized

plus

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

Make rs72556252(C;C)

Make rs72556252(C;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38401280

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556252
dbSNP (classic)	rs72556252
ClinGen	rs72556252
ebi	rs72556252
HLI	rs72556252
Exac	rs72556252
Gnomad	rs72556252
Varsome	rs72556252
LitVar	rs72556252
Map	rs72556252
PheGenI	rs72556252
Biobank	rs72556252
1000 genomes	rs72556252
hgdp	rs72556252
ensembl	rs72556252
geneview	rs72556252
scholar	rs72556252
google	rs72556252
pharmgkb	rs72556252
gwascentral	rs72556252
openSNP	rs72556252
23andMe	rs72556252
SNPshot	rs72556252
SNPdbe	rs72556252
MSV3d	rs72556252
GWAS Ctlg	rs72556252

Max Magnitude

0

ClinVar
Risk	rs72556252(C;C)
Alt	rs72556252(C;C)
Reference	Rs72556252(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38260533T>C
CLNSRC	ClinVar
CLNACC	RCV000083421.1,