rs886039853

Orientation

plus

Stabilized

plus

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

Make rs886039853(C;T)

Make rs886039853(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

9

Position

130489345

Gene

ASS1

is a	snp
is	mentioned by
dbSNP	rs886039853
dbSNP (classic)	rs886039853
ClinGen	rs886039853
ebi	rs886039853
HLI	rs886039853
Exac	rs886039853
Gnomad	rs886039853
Varsome	rs886039853
LitVar	rs886039853
Map	rs886039853
PheGenI	rs886039853
Biobank	rs886039853
1000 genomes	rs886039853
hgdp	rs886039853
ensembl	rs886039853
geneview	rs886039853
scholar	rs886039853
google	rs886039853
pharmgkb	rs886039853
gwascentral	rs886039853
openSNP	rs886039853
23andMe	rs886039853
SNPshot	rs886039853
SNPdbe	rs886039853
MSV3d	rs886039853
GWAS Ctlg	rs886039853

Max Magnitude

0

ClinVar
Risk	rs886039853(T;T)
Alt	rs886039853(T;T)
Reference	Rs886039853(C;C)
Significance	Pathogenic
Disease	Citrullinemia type I
Variation	info
Gene	ASS1
CLNDBN	Citrullinemia type I
Reversed	0
HGVS	NC_000009.11:g.133364732C>T
CLNSRC
CLNACC	RCV000256276.1,