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rs180177316

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs180177316(-;-)
Make rs180177316(-;CT)
ReferenceGRCh38 38.1/141
Chromosome9
Position37430520
GeneGRHPR
is asnp
is mentioned by
dbSNPrs180177316
ebirs180177316
HLIrs180177316
Exacrs180177316
Varsomers180177316
Maprs180177316
PheGenIrs180177316
hapmaprs180177316
1000 genomesrs180177316
hgdprs180177316
ensemblrs180177316
gopubmedrs180177316
geneviewrs180177316
scholarrs180177316
googlers180177316
pharmgkbrs180177316
gwascentralrs180177316
openSNPrs180177316
23andMers180177316
23andMe allrs180177316
SNP Nexus

SNPshotrs180177316
SNPdbers180177316
MSV3drs180177316
GWAS Ctlgrs180177316
Max Magnitude0
ClinVar
Risk rs180177316(;)
Alt rs180177316(;)
Reference rs180177316(CT;CT)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37430517_37430518delCT
CLNSRC
CLNACC RCV000186459.1,