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rs180177311

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs180177311(-;-)
Make rs180177311(-;A)
ReferenceGRCh38 38.1/141
Chromosome9
Position37422795
GeneGRHPR
is asnp
is mentioned by
dbSNPrs180177311
ebirs180177311
HLIrs180177311
Exacrs180177311
Varsomers180177311
Maprs180177311
PheGenIrs180177311
hapmaprs180177311
1000 genomesrs180177311
hgdprs180177311
ensemblrs180177311
gopubmedrs180177311
geneviewrs180177311
scholarrs180177311
googlers180177311
pharmgkbrs180177311
gwascentralrs180177311
openSNPrs180177311
23andMers180177311
23andMe allrs180177311
SNP Nexus

SNPshotrs180177311
SNPdbers180177311
MSV3drs180177311
GWAS Ctlgrs180177311
Max Magnitude0
ClinVar
Risk rs180177311(;)
Alt rs180177311(;)
Reference rs180177311(A;A)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37422792delA
CLNSRC
CLNACC RCV000186452.1,