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rs180177310

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GTAA;GTAA) 0 common in clinvar
Make rs180177310(-;-)
Make rs180177310(-;GTAA)
ReferenceGRCh38 38.1/141
Chromosome9
Position37426655
GeneGRHPR
is asnp
is mentioned by
dbSNPrs180177310
ebirs180177310
HLIrs180177310
Exacrs180177310
Varsomers180177310
Maprs180177310
PheGenIrs180177310
hapmaprs180177310
1000 genomesrs180177310
hgdprs180177310
ensemblrs180177310
gopubmedrs180177310
geneviewrs180177310
scholarrs180177310
googlers180177310
pharmgkbrs180177310
gwascentralrs180177310
openSNPrs180177310
23andMers180177310
23andMe allrs180177310
SNP Nexus

SNPshotrs180177310
SNPdbers180177310
MSV3drs180177310
GWAS Ctlgrs180177310
Max Magnitude0
ClinVar
Risk rs180177310(;)
Alt rs180177310(;)
Reference rs180177310(AAGT;AAGT)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37426654_37426657delAAGT
CLNSRC
CLNACC RCV000186457.1,