rs74518351

Orientation

plus

Stabilized

plus

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

Make rs74518351(A;G)

Make rs74518351(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38367335

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs74518351
dbSNP (classic)	rs74518351
ClinGen	rs74518351
ebi	rs74518351
HLI	rs74518351
Exac	rs74518351
Gnomad	rs74518351
Varsome	rs74518351
LitVar	rs74518351
Map	rs74518351
PheGenI	rs74518351
Biobank	rs74518351
1000 genomes	rs74518351
hgdp	rs74518351
ensembl	rs74518351
geneview	rs74518351
scholar	rs74518351
google	rs74518351
pharmgkb	rs74518351
gwascentral	rs74518351
openSNP	rs74518351
23andMe	rs74518351
SNPshot	rs74518351
SNPdbe	rs74518351
MSV3d	rs74518351
GWAS Ctlg	rs74518351

Max Magnitude

0

ClinVar
Risk	rs74518351(G;G) rs74518351(T;T)
Alt	rs74518351(G;G) rs74518351(T;T)
Reference	Rs74518351(A;A)
Significance	Pathogenic
Disease	not provided not specified
Variation	info
Gene	OTC
CLNDBN	not provided not specified
Reversed	0
HGVS	NC_000023.10:g.38226588A>G; NC_000023.10:g.38226588A>T
CLNSRC	ClinVar
CLNACC	RCV000083334.1, RCV000324897.1,