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rs180177324

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs180177324(A;G)
Make rs180177324(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position37436729
GeneGRHPR
is asnp
is mentioned by
dbSNPrs180177324
ebirs180177324
HLIrs180177324
Exacrs180177324
Varsomers180177324
Maprs180177324
PheGenIrs180177324
hapmaprs180177324
1000 genomesrs180177324
hgdprs180177324
ensemblrs180177324
gopubmedrs180177324
geneviewrs180177324
scholarrs180177324
googlers180177324
pharmgkbrs180177324
gwascentralrs180177324
openSNPrs180177324
23andMers180177324
23andMe allrs180177324
SNP Nexus

SNPshotrs180177324
SNPdbers180177324
MSV3drs180177324
GWAS Ctlgrs180177324
Max Magnitude0
ClinVar
Risk rs180177324(G;G)
Alt rs180177324(G;G)
Reference rs180177324(A;A)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37436726A>G
CLNSRC
CLNACC RCV000186445.1,