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rs180177307

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177307(A;A)
Make rs180177307(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position37426587
GeneGRHPR
is asnp
is mentioned by
dbSNPrs180177307
ebirs180177307
HLIrs180177307
Exacrs180177307
Varsomers180177307
Maprs180177307
PheGenIrs180177307
hapmaprs180177307
1000 genomesrs180177307
hgdprs180177307
ensemblrs180177307
gopubmedrs180177307
geneviewrs180177307
scholarrs180177307
googlers180177307
pharmgkbrs180177307
gwascentralrs180177307
openSNPrs180177307
23andMers180177307
23andMe allrs180177307
SNP Nexus

SNPshotrs180177307
SNPdbers180177307
MSV3drs180177307
GWAS Ctlgrs180177307
Max Magnitude0
ClinVar
Risk rs180177307(A;A)
Alt rs180177307(A;A)
Reference rs180177307(G;G)
Significance Other
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37426584G>A
CLNSRC
CLNACC RCV000169087.2,