Have questions? Visit https://www.reddit.com/r/SNPedia

rs180177314

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177314(A;A)
Make rs180177314(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position37429732
GeneGRHPR
is asnp
is mentioned by
dbSNPrs180177314
ebirs180177314
HLIrs180177314
Exacrs180177314
Varsomers180177314
Maprs180177314
PheGenIrs180177314
hapmaprs180177314
1000 genomesrs180177314
hgdprs180177314
ensemblrs180177314
gopubmedrs180177314
geneviewrs180177314
scholarrs180177314
googlers180177314
pharmgkbrs180177314
gwascentralrs180177314
openSNPrs180177314
23andMers180177314
23andMe allrs180177314
SNP Nexus

SNPshotrs180177314
SNPdbers180177314
MSV3drs180177314
GWAS Ctlgrs180177314
Max Magnitude0
ClinVar
Risk rs180177314(A;A)
Alt rs180177314(A;A)
Reference rs180177314(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37429729G>A
CLNSRC
CLNACC RCV000186442.1,