rs767405535

Orientation

plus

Stabilized

plus

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

Make rs767405535(C;T)

Make rs767405535(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

97599094

Gene

HOGA1

is a	snp
is	mentioned by
dbSNP	rs767405535
dbSNP (classic)	rs767405535
ClinGen	rs767405535
ebi	rs767405535
HLI	rs767405535
Exac	rs767405535
Gnomad	rs767405535
Varsome	rs767405535
LitVar	rs767405535
Map	rs767405535
PheGenI	rs767405535
Biobank	rs767405535
1000 genomes	rs767405535
hgdp	rs767405535
ensembl	rs767405535
geneview	rs767405535
scholar	rs767405535
google	rs767405535
pharmgkb	rs767405535
gwascentral	rs767405535
openSNP	rs767405535
23andMe	rs767405535
SNPshot	rs767405535
SNPdbe	rs767405535
MSV3d	rs767405535
GWAS Ctlg	rs767405535

Max Magnitude

0

ClinVar
Risk	rs767405535(A;A) rs767405535(T;T)
Alt	rs767405535(A;A) rs767405535(T;T)
Reference	Rs767405535(C;C)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	HOGA1
CLNDBN	Primary hyperoxaluria, type III
Reversed	0
HGVS	NC_000010.10:g.99358851C>T
CLNSRC
CLNACC	RCV000186478.1,