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rs180177308

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177308(-;-)
Make rs180177308(-;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position37426625
GeneGRHPR
is asnp
is mentioned by
dbSNPrs180177308
ebirs180177308
HLIrs180177308
Exacrs180177308
Varsomers180177308
Maprs180177308
PheGenIrs180177308
hapmaprs180177308
1000 genomesrs180177308
hgdprs180177308
ensemblrs180177308
gopubmedrs180177308
geneviewrs180177308
scholarrs180177308
googlers180177308
pharmgkbrs180177308
gwascentralrs180177308
openSNPrs180177308
23andMers180177308
23andMe allrs180177308
SNP Nexus

SNPshotrs180177308
SNPdbers180177308
MSV3drs180177308
GWAS Ctlgrs180177308
Max Magnitude0
ClinVar
Risk rs180177308(;)
Alt rs180177308(;)
Reference rs180177308(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37426622delG
CLNSRC
CLNACC RCV000186456.1,