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rs180177304

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177304(A;A)
Make rs180177304(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position37424863
GeneGRHPR
is asnp
is mentioned by
dbSNPrs180177304
ebirs180177304
HLIrs180177304
Exacrs180177304
Varsomers180177304
Maprs180177304
PheGenIrs180177304
hapmaprs180177304
1000 genomesrs180177304
hgdprs180177304
ensemblrs180177304
gopubmedrs180177304
geneviewrs180177304
scholarrs180177304
googlers180177304
pharmgkbrs180177304
gwascentralrs180177304
openSNPrs180177304
23andMers180177304
23andMe allrs180177304
SNP Nexus

SNPshotrs180177304
SNPdbers180177304
MSV3drs180177304
GWAS Ctlgrs180177304
Max Magnitude0
ClinVar
Risk rs180177304(A;A)
Alt rs180177304(A;A)
Reference rs180177304(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37424860G>A
CLNSRC
CLNACC RCV000186438.1,