rs180177307

Orientation

plus

Stabilized

plus

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

Make rs180177307(A;A)

Make rs180177307(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

37426587

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs180177307
dbSNP (classic)	rs180177307
ClinGen	rs180177307
ebi	rs180177307
HLI	rs180177307
Exac	rs180177307
Gnomad	rs180177307
Varsome	rs180177307
LitVar	rs180177307
Map	rs180177307
PheGenI	rs180177307
Biobank	rs180177307
1000 genomes	rs180177307
hgdp	rs180177307
ensembl	rs180177307
geneview	rs180177307
scholar	rs180177307
google	rs180177307
pharmgkb	rs180177307
gwascentral	rs180177307
openSNP	rs180177307
23andMe	rs180177307
SNPshot	rs180177307
SNPdbe	rs180177307
MSV3d	rs180177307
GWAS Ctlg	rs180177307

Max Magnitude

0

ClinVar
Risk	rs180177307(A;A) rs180177307(T;T)
Alt	rs180177307(A;A) rs180177307(T;T)
Reference	Rs180177307(G;G)
Significance	Other
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37426584G>A; NC_000009.11:g.37426584G>T
CLNSRC
CLNACC	RCV000169087.2, RCV000412226.1,