rs777601935

Orientation

plus

Stabilized

plus

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

Make rs777601935(C;C)

Make rs777601935(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

97599740

Gene

HOGA1

is a	snp
is	mentioned by
dbSNP	rs777601935
dbSNP (classic)	rs777601935
ClinGen	rs777601935
ebi	rs777601935
HLI	rs777601935
Exac	rs777601935
Gnomad	rs777601935
Varsome	rs777601935
LitVar	rs777601935
Map	rs777601935
PheGenI	rs777601935
Biobank	rs777601935
1000 genomes	rs777601935
hgdp	rs777601935
ensembl	rs777601935
geneview	rs777601935
scholar	rs777601935
google	rs777601935
pharmgkb	rs777601935
gwascentral	rs777601935
openSNP	rs777601935
23andMe	rs777601935
SNPshot	rs777601935
SNPdbe	rs777601935
MSV3d	rs777601935
GWAS Ctlg	rs777601935

Max Magnitude

0

ClinVar
Risk	rs777601935(C;C) rs777601935(T;T)
Alt	rs777601935(C;C) rs777601935(T;T)
Reference	Rs777601935(G;G)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	HOGA1
CLNDBN	Primary hyperoxaluria, type III
Reversed	0
HGVS	NC_000010.10:g.99359497G>T
CLNSRC
CLNACC	RCV000186479.1,