rs72556285

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(ACGCTC;ACGCTC)	0	common in clinvar
(CTCACG;CTCACG)	0	common in clinvar
(I;I)	0

Make rs72556285(-;-)

Make rs72556285(-;ACGCTC)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38401420

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556285
dbSNP (classic)	rs72556285
ClinGen	rs72556285
ebi	rs72556285
HLI	rs72556285
Exac	rs72556285
Gnomad	rs72556285
Varsome	rs72556285
LitVar	rs72556285
Map	rs72556285
PheGenI	rs72556285
Biobank	rs72556285
1000 genomes	rs72556285
hgdp	rs72556285
ensembl	rs72556285
geneview	rs72556285
scholar	rs72556285
google	rs72556285
pharmgkb	rs72556285
gwascentral	rs72556285
openSNP	rs72556285
23andMe	rs72556285
SNPshot	rs72556285
SNPdbe	rs72556285
MSV3d	rs72556285
GWAS Ctlg	rs72556285

Max Magnitude

0

ClinVar
Risk	rs72556285(-;-)
Alt	rs72556285(-;-)
Reference	Rs72556285(CTCACG;CTCACG)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38260673_38260678delACGCTC
CLNSRC	ClinVar
CLNACC	RCV000083476.1,