rs111060774

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(GCTCTTTACATGTAAA;GCTCTTTACATGTAAA)	0	common in clinvar
(TCTTTACATGTAAAGC;TCTTTACATGTAAAGC)	0	common in clinvar

Make rs111060774(-;-)

Make rs111060774(-;TCTTTACATGTAAAGC)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38408802

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs111060774
dbSNP (classic)	rs111060774
ClinGen	rs111060774
ebi	rs111060774
HLI	rs111060774
Exac	rs111060774
Gnomad	rs111060774
Varsome	rs111060774
LitVar	rs111060774
Map	rs111060774
PheGenI	rs111060774
Biobank	rs111060774
1000 genomes	rs111060774
hgdp	rs111060774
ensembl	rs111060774
geneview	rs111060774
scholar	rs111060774
google	rs111060774
pharmgkb	rs111060774
gwascentral	rs111060774
openSNP	rs111060774
23andMe	rs111060774
SNPshot	rs111060774
SNPdbe	rs111060774
MSV3d	rs111060774
GWAS Ctlg	rs111060774

Max Magnitude

0

ClinVar
Risk	rs111060774(-;-)
Alt	rs111060774(-;-)
Reference	Rs111060774(GCTCTTTACATGTAAA;GCTCTTTACATGTAAA)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38268055_38268070del16
CLNSRC	ClinVar
CLNACC	RCV000083546.1,