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rs180177312

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177312(A;A)
Make rs180177312(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position37428557
GeneGRHPR
is asnp
is mentioned by
dbSNPrs180177312
ebirs180177312
HLIrs180177312
Exacrs180177312
Varsomers180177312
Maprs180177312
PheGenIrs180177312
hapmaprs180177312
1000 genomesrs180177312
hgdprs180177312
ensemblrs180177312
gopubmedrs180177312
geneviewrs180177312
scholarrs180177312
googlers180177312
pharmgkbrs180177312
gwascentralrs180177312
openSNPrs180177312
23andMers180177312
23andMe allrs180177312
SNP Nexus

SNPshotrs180177312
SNPdbers180177312
MSV3drs180177312
GWAS Ctlgrs180177312
Max Magnitude0
ClinVar
Risk rs180177312(A;A)
Alt rs180177312(A;A)
Reference rs180177312(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37428554G>A
CLNSRC
CLNACC RCV000186441.1,