rs770050262

Orientation

plus

Stabilized

plus

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

Make rs770050262(G;T)

Make rs770050262(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

97601990

Gene

HOGA1

is a	snp
is	mentioned by
dbSNP	rs770050262
dbSNP (classic)	rs770050262
ClinGen	rs770050262
ebi	rs770050262
HLI	rs770050262
Exac	rs770050262
Gnomad	rs770050262
Varsome	rs770050262
LitVar	rs770050262
Map	rs770050262
PheGenI	rs770050262
Biobank	rs770050262
1000 genomes	rs770050262
hgdp	rs770050262
ensembl	rs770050262
geneview	rs770050262
scholar	rs770050262
google	rs770050262
pharmgkb	rs770050262
gwascentral	rs770050262
openSNP	rs770050262
23andMe	rs770050262
SNPshot	rs770050262
SNPdbe	rs770050262
MSV3d	rs770050262
GWAS Ctlg	rs770050262

Max Magnitude

0

ClinVar
Risk	rs770050262(A;A) rs770050262(T;T)
Alt	rs770050262(A;A) rs770050262(T;T)
Reference	Rs770050262(G;G)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	HOGA1
CLNDBN	Primary hyperoxaluria, type III
Reversed	0
HGVS	NC_000010.10:g.99361747G>A
CLNSRC
CLNACC	RCV000186493.1,