rs796052092

Orientation

plus

Stabilized

plus

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

Make rs796052092(-;-)

Make rs796052092(-;TGC)

Make rs796052092(TGC;TGC)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

97601959

Gene

HOGA1

is a	snp
is	mentioned by
dbSNP	rs796052092
dbSNP (classic)	rs796052092
ClinGen	rs796052092
ebi	rs796052092
HLI	rs796052092
Exac	rs796052092
Gnomad	rs796052092
Varsome	rs796052092
LitVar	rs796052092
Map	rs796052092
PheGenI	rs796052092
Biobank	rs796052092
1000 genomes	rs796052092
hgdp	rs796052092
ensembl	rs796052092
geneview	rs796052092
scholar	rs796052092
google	rs796052092
pharmgkb	rs796052092
gwascentral	rs796052092
openSNP	rs796052092
23andMe	rs796052092
SNPshot	rs796052092
SNPdbe	rs796052092
MSV3d	rs796052092
GWAS Ctlg	rs796052092

Max Magnitude

0

ClinVar
Risk	rs796052092(-;-)
Alt	rs796052092(-;-)
Reference	Rs796052092(CTG;CTG)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	HOGA1
CLNDBN	Primary hyperoxaluria, type III
Reversed	0
HGVS	NC_000010.10:g.99361716_99361718delTGC
CLNSRC
CLNACC	RCV000186495.1,