rs67870244

Orientation

plus

Stabilized

plus

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

Make rs67870244(C;G)

Make rs67870244(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38411900

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs67870244
dbSNP (classic)	rs67870244
ClinGen	rs67870244
ebi	rs67870244
HLI	rs67870244
Exac	rs67870244
Gnomad	rs67870244
Varsome	rs67870244
LitVar	rs67870244
Map	rs67870244
PheGenI	rs67870244
Biobank	rs67870244
1000 genomes	rs67870244
hgdp	rs67870244
ensembl	rs67870244
geneview	rs67870244
scholar	rs67870244
google	rs67870244
pharmgkb	rs67870244
gwascentral	rs67870244
openSNP	rs67870244
23andMe	rs67870244
SNPshot	rs67870244
SNPdbe	rs67870244
MSV3d	rs67870244
GWAS Ctlg	rs67870244

Max Magnitude

0

ClinVar
Risk	rs67870244(G;G)
Alt	rs67870244(G;G)
Reference	Rs67870244(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38271153C>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000083602.1,