rs267606763

Orientation

plus

Stabilized

plus

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

Make rs267606763(C;C)

Make rs267606763(C;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

97584912

Gene

HOGA1

is a	snp
is	mentioned by
dbSNP	rs267606763
dbSNP (classic)	rs267606763
ClinGen	rs267606763
ebi	rs267606763
HLI	rs267606763
Exac	rs267606763
Gnomad	rs267606763
Varsome	rs267606763
LitVar	rs267606763
Map	rs267606763
PheGenI	rs267606763
Biobank	rs267606763
1000 genomes	rs267606763
hgdp	rs267606763
ensembl	rs267606763
geneview	rs267606763
scholar	rs267606763
google	rs267606763
pharmgkb	rs267606763
gwascentral	rs267606763
openSNP	rs267606763
23andMe	rs267606763
SNPshot	rs267606763
SNPdbe	rs267606763
MSV3d	rs267606763
GWAS Ctlg	rs267606763

Max Magnitude

0

ClinVar
Risk	rs267606763(A;A) rs267606763(C;C)
Alt	rs267606763(A;A) rs267606763(C;C)
Reference	Rs267606763(G;G)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	HOGA1
CLNDBN	Primary hyperoxaluria, type III
Reversed	0
HGVS	NC_000010.10:g.99344669G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000050.2,