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rs180177323

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177323(A;A)
Make rs180177323(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position37436700
GeneGRHPR
is asnp
is mentioned by
dbSNPrs180177323
ebirs180177323
HLIrs180177323
Exacrs180177323
Varsomers180177323
Maprs180177323
PheGenIrs180177323
hapmaprs180177323
1000 genomesrs180177323
hgdprs180177323
ensemblrs180177323
gopubmedrs180177323
geneviewrs180177323
scholarrs180177323
googlers180177323
pharmgkbrs180177323
gwascentralrs180177323
openSNPrs180177323
23andMers180177323
23andMe allrs180177323
SNP Nexus

SNPshotrs180177323
SNPdbers180177323
MSV3drs180177323
GWAS Ctlgrs180177323
Max Magnitude0
ClinVar
Risk rs180177323(A;A)
Alt rs180177323(A;A)
Reference rs180177323(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37436697G>A
CLNSRC
CLNACC RCV000186444.1,