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rs180177313

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs180177313(A;A)
Make rs180177313(A;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position37428574
GeneGRHPR
is asnp
is mentioned by
dbSNPrs180177313
ebirs180177313
HLIrs180177313
Exacrs180177313
Varsomers180177313
Maprs180177313
PheGenIrs180177313
hapmaprs180177313
1000 genomesrs180177313
hgdprs180177313
ensemblrs180177313
gopubmedrs180177313
geneviewrs180177313
scholarrs180177313
googlers180177313
pharmgkbrs180177313
gwascentralrs180177313
openSNPrs180177313
23andMers180177313
23andMe allrs180177313
SNP Nexus

SNPshotrs180177313
SNPdbers180177313
MSV3drs180177313
GWAS Ctlgrs180177313
Max Magnitude0
ClinVar
Risk rs180177313(A;A)
Alt rs180177313(A;A)
Reference rs180177313(T;T)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37428571T>A
CLNSRC
CLNACC RCV000186450.1,