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rs180177305

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs180177305(C;C)
Make rs180177305(C;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position37424964
GeneGRHPR
is asnp
is mentioned by
dbSNPrs180177305
ebirs180177305
HLIrs180177305
Exacrs180177305
Varsomers180177305
Maprs180177305
PheGenIrs180177305
hapmaprs180177305
1000 genomesrs180177305
hgdprs180177305
ensemblrs180177305
gopubmedrs180177305
geneviewrs180177305
scholarrs180177305
googlers180177305
pharmgkbrs180177305
gwascentralrs180177305
openSNPrs180177305
23andMers180177305
23andMe allrs180177305
SNP Nexus

SNPshotrs180177305
SNPdbers180177305
MSV3drs180177305
GWAS Ctlgrs180177305
Max Magnitude0
ClinVar
Risk rs180177305(C;C)
Alt rs180177305(C;C)
Reference rs180177305(T;T)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37424961T>C
CLNSRC
CLNACC RCV000186439.1,