rs777046879

Orientation

plus

Stabilized

plus

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

Make rs777046879(A;A)

Make rs777046879(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

97611648

Gene

HOGA1

is a	snp
is	mentioned by
dbSNP	rs777046879
dbSNP (classic)	rs777046879
ClinGen	rs777046879
ebi	rs777046879
HLI	rs777046879
Exac	rs777046879
Gnomad	rs777046879
Varsome	rs777046879
LitVar	rs777046879
Map	rs777046879
PheGenI	rs777046879
Biobank	rs777046879
1000 genomes	rs777046879
hgdp	rs777046879
ensembl	rs777046879
geneview	rs777046879
scholar	rs777046879
google	rs777046879
pharmgkb	rs777046879
gwascentral	rs777046879
openSNP	rs777046879
23andMe	rs777046879
SNPshot	rs777046879
SNPdbe	rs777046879
MSV3d	rs777046879
GWAS Ctlg	rs777046879

Max Magnitude

0

ClinVar
Risk	rs777046879(A;A)
Alt	rs777046879(A;A)
Reference	Rs777046879(G;G)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	HOGA1
CLNDBN	Primary hyperoxaluria, type III
Reversed	0
HGVS	NC_000010.10:g.99371405G>A
CLNSRC
CLNACC	RCV000186491.1,