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rs180177321

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs180177321(-;-)
Make rs180177321(-;TG)
ReferenceGRCh38 38.1/141
Chromosome9
Position37432137
GeneGRHPR
is asnp
is mentioned by
dbSNPrs180177321
ebirs180177321
HLIrs180177321
Exacrs180177321
Varsomers180177321
Maprs180177321
PheGenIrs180177321
hapmaprs180177321
1000 genomesrs180177321
hgdprs180177321
ensemblrs180177321
gopubmedrs180177321
geneviewrs180177321
scholarrs180177321
googlers180177321
pharmgkbrs180177321
gwascentralrs180177321
openSNPrs180177321
23andMers180177321
23andMe allrs180177321
SNP Nexus

SNPshotrs180177321
SNPdbers180177321
MSV3drs180177321
GWAS Ctlgrs180177321
Max Magnitude0
ClinVar
Risk rs180177321(;)
Alt rs180177321(;)
Reference rs180177321(TG;TG)
Significance Other
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37432134_37432135delTG
CLNSRC OMIM Allelic Variant
CLNACC RCV000149441.7,