rs72556251

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(I;I)	0

Make rs72556251(-;TTA)

Make rs72556251(TTA;TTA)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38401278

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556251
dbSNP (classic)	rs72556251
ClinGen	rs72556251
ebi	rs72556251
HLI	rs72556251
Exac	rs72556251
Gnomad	rs72556251
Varsome	rs72556251
LitVar	rs72556251
Map	rs72556251
PheGenI	rs72556251
Biobank	rs72556251
1000 genomes	rs72556251
hgdp	rs72556251
ensembl	rs72556251
geneview	rs72556251
scholar	rs72556251
google	rs72556251
pharmgkb	rs72556251
gwascentral	rs72556251
openSNP	rs72556251
23andMe	rs72556251
SNPshot	rs72556251
SNPdbe	rs72556251
MSV3d	rs72556251
GWAS Ctlg	rs72556251

Max Magnitude

0

ClinVar
Risk	rs72556251(TAT;TAT)
Alt	rs72556251(TAT;TAT)
Reference	Rs72556251(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38260531_38260532insTTA
CLNSRC	ClinVar
CLNACC	RCV000083420.1,