rs764396564

Orientation

plus

Stabilized

plus

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

Make rs764396564(C;T)

Make rs764396564(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

97584837

Gene

HOGA1

is a	snp
is	mentioned by
dbSNP	rs764396564
dbSNP (classic)	rs764396564
ClinGen	rs764396564
ebi	rs764396564
HLI	rs764396564
Exac	rs764396564
Gnomad	rs764396564
Varsome	rs764396564
LitVar	rs764396564
Map	rs764396564
PheGenI	rs764396564
Biobank	rs764396564
1000 genomes	rs764396564
hgdp	rs764396564
ensembl	rs764396564
geneview	rs764396564
scholar	rs764396564
google	rs764396564
pharmgkb	rs764396564
gwascentral	rs764396564
openSNP	rs764396564
23andMe	rs764396564
SNPshot	rs764396564
SNPdbe	rs764396564
MSV3d	rs764396564
GWAS Ctlg	rs764396564

Max Magnitude

0

ClinVar
Risk	rs764396564(T;T)
Alt	rs764396564(T;T)
Reference	Rs764396564(C;C)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	HOGA1
CLNDBN	Primary hyperoxaluria, type III
Reversed	0
HGVS	NC_000010.10:g.99344594C>T
CLNSRC
CLNACC	RCV000186473.1,