rs180177313

Orientation

plus

Stabilized

plus

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

Make rs180177313(A;A)

Make rs180177313(A;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

37428574

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs180177313
dbSNP (classic)	rs180177313
ClinGen	rs180177313
ebi	rs180177313
HLI	rs180177313
Exac	rs180177313
Gnomad	rs180177313
Varsome	rs180177313
LitVar	rs180177313
Map	rs180177313
PheGenI	rs180177313
Biobank	rs180177313
1000 genomes	rs180177313
hgdp	rs180177313
ensembl	rs180177313
geneview	rs180177313
scholar	rs180177313
google	rs180177313
pharmgkb	rs180177313
gwascentral	rs180177313
openSNP	rs180177313
23andMe	rs180177313
SNPshot	rs180177313
SNPdbe	rs180177313
MSV3d	rs180177313
GWAS Ctlg	rs180177313

Max Magnitude

0

ClinVar
Risk	rs180177313(A;A)
Alt	rs180177313(A;A)
Reference	Rs180177313(T;T)
Significance	Other
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37428571T>A
CLNSRC
CLNACC	RCV000186450.1,