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rs180177325

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs180177325(C;C)
Make rs180177325(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position37436760
GeneGRHPR
is asnp
is mentioned by
dbSNPrs180177325
ebirs180177325
HLIrs180177325
Exacrs180177325
Varsomers180177325
Maprs180177325
PheGenIrs180177325
hapmaprs180177325
1000 genomesrs180177325
hgdprs180177325
ensemblrs180177325
gopubmedrs180177325
geneviewrs180177325
scholarrs180177325
googlers180177325
pharmgkbrs180177325
gwascentralrs180177325
openSNPrs180177325
23andMers180177325
23andMe allrs180177325
SNP Nexus

SNPshotrs180177325
SNPdbers180177325
MSV3drs180177325
GWAS Ctlgrs180177325
Max Magnitude0
ClinVar
Risk rs180177325(C,G;C,G)
Alt rs180177325(C,G;C,G)
Reference rs180177325(T;T)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37436757T>C; NC_000009.11:g.37436757T>G
CLNSRC
CLNACC RCV000186447.1, RCV000186446.1,