rs181509591

Orientation

plus

Stabilized

plus

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

Make rs181509591(A;A)

Make rs181509591(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

4

Position

9996817

Gene	LOC105374476, SLC2A9

is a	snp
is	mentioned by
dbSNP	rs181509591
dbSNP (classic)	rs181509591
ClinGen	rs181509591
ebi	rs181509591
HLI	rs181509591
Exac	rs181509591
Gnomad	rs181509591
Varsome	rs181509591
LitVar	rs181509591
Map	rs181509591
PheGenI	rs181509591
Biobank	rs181509591
1000 genomes	rs181509591
hgdp	rs181509591
ensembl	rs181509591
geneview	rs181509591
scholar	rs181509591
google	rs181509591
pharmgkb	rs181509591
gwascentral	rs181509591
openSNP	rs181509591
23andMe	rs181509591
SNPshot	rs181509591
SNPdbe	rs181509591
MSV3d	rs181509591
GWAS Ctlg	rs181509591

Max Magnitude

0

ClinVar
Risk	rs181509591(A;A) rs181509591(C;C)
Alt	rs181509591(A;A) rs181509591(C;C)
Reference	Rs181509591(G;G)
Significance	Pathogenic
Disease	Renal hypouricemia 2
Variation	info
Gene	SLC2A9
CLNDBN	Renal hypouricemia 2
Reversed	0
HGVS	NC_000004.11:g.9998441G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000201283.1,