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rs180177315

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs180177315(-;-)
Make rs180177315(-;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position37429778
GeneGRHPR
is asnp
is mentioned by
dbSNPrs180177315
ebirs180177315
HLIrs180177315
Exacrs180177315
Varsomers180177315
Maprs180177315
PheGenIrs180177315
hapmaprs180177315
1000 genomesrs180177315
hgdprs180177315
ensemblrs180177315
gopubmedrs180177315
geneviewrs180177315
scholarrs180177315
googlers180177315
pharmgkbrs180177315
gwascentralrs180177315
openSNPrs180177315
23andMers180177315
23andMe allrs180177315
SNP Nexus

SNPshotrs180177315
SNPdbers180177315
MSV3drs180177315
GWAS Ctlgrs180177315
Max Magnitude0
ClinVar
Risk rs180177315(;)
Alt rs180177315(;)
Reference rs180177315(T;T)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37429775delT
CLNSRC
CLNACC RCV000186458.1,