rs672601351

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common genotype
(TG;TG)	0	common in clinvar

Make rs672601351(-;-)

Make rs672601351(-;TG)

Reference

GRCh38.p2 38.2/144

Chromosome

9

Position

37425955

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs672601351
dbSNP (classic)	rs672601351
ClinGen	rs672601351
ebi	rs672601351
HLI	rs672601351
Exac	rs672601351
Gnomad	rs672601351
Varsome	rs672601351
LitVar	rs672601351
Map	rs672601351
PheGenI	rs672601351
Biobank	rs672601351
1000 genomes	rs672601351
hgdp	rs672601351
ensembl	rs672601351
geneview	rs672601351
scholar	rs672601351
google	rs672601351
pharmgkb	rs672601351
gwascentral	rs672601351
openSNP	rs672601351
23andMe	rs672601351
SNPshot	rs672601351
SNPdbe	rs672601351
MSV3d	rs672601351
GWAS Ctlg	rs672601351

Max Magnitude

0

ClinVar
Risk	rs672601351(-;-)
Alt	rs672601351(-;-)
Reference	Rs672601351(TG;TG)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37425952_37425953delTG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000149442.5,