rs72554315

Orientation

plus

Stabilized

plus

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

Make rs72554315(C;C)

Make rs72554315(C;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38367356

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72554315
dbSNP (classic)	rs72554315
ClinGen	rs72554315
ebi	rs72554315
HLI	rs72554315
Exac	rs72554315
Gnomad	rs72554315
Varsome	rs72554315
LitVar	rs72554315
Map	rs72554315
PheGenI	rs72554315
Biobank	rs72554315
1000 genomes	rs72554315
hgdp	rs72554315
ensembl	rs72554315
geneview	rs72554315
scholar	rs72554315
google	rs72554315
pharmgkb	rs72554315
gwascentral	rs72554315
openSNP	rs72554315
23andMe	rs72554315
SNPshot	rs72554315
SNPdbe	rs72554315
MSV3d	rs72554315
GWAS Ctlg	rs72554315

Max Magnitude

0

ClinVar
Risk	rs72554315(C;C)
Alt	rs72554315(C;C)
Reference	Rs72554315(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38226609T>C
CLNSRC	ClinVar
CLNACC	RCV000083343.1,