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rs180177322

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs180177322(C;T)
Make rs180177322(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position37436699
GeneGRHPR
is asnp
is mentioned by
dbSNPrs180177322
ebirs180177322
HLIrs180177322
Exacrs180177322
Varsomers180177322
Maprs180177322
PheGenIrs180177322
hapmaprs180177322
1000 genomesrs180177322
hgdprs180177322
ensemblrs180177322
gopubmedrs180177322
geneviewrs180177322
scholarrs180177322
googlers180177322
pharmgkbrs180177322
gwascentralrs180177322
openSNPrs180177322
23andMers180177322
23andMe allrs180177322
SNP Nexus

SNPshotrs180177322
SNPdbers180177322
MSV3drs180177322
GWAS Ctlgrs180177322
Max Magnitude0
ClinVar
Risk rs180177322(T;T)
Alt rs180177322(T;T)
Reference rs180177322(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37436696C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000149443.5,