rs183276875

Orientation

plus

Stabilized

plus

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

Make rs183276875(C;T)

Make rs183276875(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

9

Position

130489413

Gene

ASS1

is a	snp
is	mentioned by
dbSNP	rs183276875
dbSNP (classic)	rs183276875
ClinGen	rs183276875
ebi	rs183276875
HLI	rs183276875
Exac	rs183276875
Gnomad	rs183276875
Varsome	rs183276875
LitVar	rs183276875
Map	rs183276875
PheGenI	rs183276875
Biobank	rs183276875
1000 genomes	rs183276875
hgdp	rs183276875
ensembl	rs183276875
geneview	rs183276875
scholar	rs183276875
google	rs183276875
pharmgkb	rs183276875
gwascentral	rs183276875
openSNP	rs183276875
23andMe	rs183276875
SNPshot	rs183276875
SNPdbe	rs183276875
MSV3d	rs183276875
GWAS Ctlg	rs183276875

Max Magnitude

0

ClinVar
Risk	rs183276875(T;T)
Alt	rs183276875(T;T)
Reference	Rs183276875(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ASS1
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.133364800C>T
CLNSRC
CLNACC	RCV000255358.1,