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rs180177317

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177317(A;A)
Make rs180177317(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position37432007
GeneGRHPR
is asnp
is mentioned by
dbSNPrs180177317
ebirs180177317
HLIrs180177317
Exacrs180177317
Varsomers180177317
Maprs180177317
PheGenIrs180177317
hapmaprs180177317
1000 genomesrs180177317
hgdprs180177317
ensemblrs180177317
gopubmedrs180177317
geneviewrs180177317
scholarrs180177317
googlers180177317
pharmgkbrs180177317
gwascentralrs180177317
openSNPrs180177317
23andMers180177317
23andMe allrs180177317
SNP Nexus

SNPshotrs180177317
SNPdbers180177317
MSV3drs180177317
GWAS Ctlgrs180177317
Max Magnitude0
ClinVar
Risk rs180177317(A;A)
Alt rs180177317(A;A)
Reference rs180177317(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37432004G>A
CLNSRC
CLNACC RCV000186451.1,