rs267606762

Orientation

plus

Stabilized

plus

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

Make rs267606762(C;T)

Make rs267606762(T;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

97598852

Gene

HOGA1

is a	snp
is	mentioned by
dbSNP	rs267606762
dbSNP (classic)	rs267606762
ClinGen	rs267606762
ebi	rs267606762
HLI	rs267606762
Exac	rs267606762
Gnomad	rs267606762
Varsome	rs267606762
LitVar	rs267606762
Map	rs267606762
PheGenI	rs267606762
Biobank	rs267606762
1000 genomes	rs267606762
hgdp	rs267606762
ensembl	rs267606762
geneview	rs267606762
scholar	rs267606762
google	rs267606762
pharmgkb	rs267606762
gwascentral	rs267606762
openSNP	rs267606762
23andMe	rs267606762
SNPshot	rs267606762
SNPdbe	rs267606762
MSV3d	rs267606762
GWAS Ctlg	rs267606762

Max Magnitude

0

ClinVar
Risk	rs267606762(T;T)
Alt	rs267606762(T;T)
Reference	Rs267606762(C;C)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	HOGA1
CLNDBN	Primary hyperoxaluria, type III
Reversed	0
HGVS	NC_000010.10:g.99358609C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000048.2,