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rs180177319

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs180177319(A;G)
Make rs180177319(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position37424843
GeneGRHPR
is asnp
is mentioned by
dbSNPrs180177319
ebirs180177319
HLIrs180177319
Exacrs180177319
Varsomers180177319
Maprs180177319
PheGenIrs180177319
hapmaprs180177319
1000 genomesrs180177319
hgdprs180177319
ensemblrs180177319
gopubmedrs180177319
geneviewrs180177319
scholarrs180177319
googlers180177319
pharmgkbrs180177319
gwascentralrs180177319
openSNPrs180177319
23andMers180177319
23andMe allrs180177319
SNP Nexus

SNPshotrs180177319
SNPdbers180177319
MSV3drs180177319
GWAS Ctlgrs180177319
Max Magnitude0
ClinVar
Risk rs180177319(G;G)
Alt rs180177319(G;G)
Reference rs180177319(A;A)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37424840A>G
CLNSRC
CLNACC RCV000186448.1,