rs121908637

Orientation

plus

Stabilized

plus

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

Make rs121908637(A;A)

Make rs121908637(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

130466774

Gene

ASS1

is a	snp
is	mentioned by
dbSNP	rs121908637
dbSNP (classic)	rs121908637
ClinGen	rs121908637
ebi	rs121908637
HLI	rs121908637
Exac	rs121908637
Gnomad	rs121908637
Varsome	rs121908637
LitVar	rs121908637
Map	rs121908637
PheGenI	rs121908637
Biobank	rs121908637
1000 genomes	rs121908637
hgdp	rs121908637
ensembl	rs121908637
geneview	rs121908637
scholar	rs121908637
google	rs121908637
pharmgkb	rs121908637
gwascentral	rs121908637
openSNP	rs121908637
23andMe	rs121908637
SNPshot	rs121908637
SNPdbe	rs121908637
MSV3d	rs121908637
GWAS Ctlg	rs121908637

Max Magnitude

0

OMIM	603470
Desc
Variant	0005
Related	also

ClinVar
Risk	rs121908637(A;A)
Alt	rs121908637(A;A)
Reference	Rs121908637(G;G)
Significance	Pathogenic
Disease	Citrullinemia type I not specified
Variation	info
Gene	ASS1
CLNDBN	Citrullinemia type I not specified
Reversed	0
HGVS	NC_000009.11:g.133342161G>A
CLNSRC	HGMD OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006697.2, RCV000259104.1,