rs374327791

Orientation

plus

Stabilized

plus

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

Make rs374327791(C;T)

Make rs374327791(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

97599746

Gene

HOGA1

is a	snp
is	mentioned by
dbSNP	rs374327791
dbSNP (classic)	rs374327791
ClinGen	rs374327791
ebi	rs374327791
HLI	rs374327791
Exac	rs374327791
Gnomad	rs374327791
Varsome	rs374327791
LitVar	rs374327791
Map	rs374327791
PheGenI	rs374327791
Biobank	rs374327791
1000 genomes	rs374327791
hgdp	rs374327791
ensembl	rs374327791
geneview	rs374327791
scholar	rs374327791
google	rs374327791
pharmgkb	rs374327791
gwascentral	rs374327791
openSNP	rs374327791
23andMe	rs374327791
SNPshot	rs374327791
SNPdbe	rs374327791
MSV3d	rs374327791
GWAS Ctlg	rs374327791

Max Magnitude

0

ClinVar
Risk	rs374327791(A;A) rs374327791(T;T)
Alt	rs374327791(A;A) rs374327791(T;T)
Reference	Rs374327791(C;C)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	HOGA1
CLNDBN	Primary hyperoxaluria, type III
Reversed	0
HGVS	NC_000010.10:g.99359503C>A
CLNSRC
CLNACC	RCV000186490.1,