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rs796052082

From SNPedia

Orientationplus
Make rs796052082(-;-)
Make rs796052082(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position37430606
GeneGRHPR
is asnp
is mentioned by
dbSNPrs796052082
ebirs796052082
HLIrs796052082
Exacrs796052082
Varsomers796052082
Maprs796052082
PheGenIrs796052082
hapmaprs796052082
1000 genomesrs796052082
hgdprs796052082
ensemblrs796052082
gopubmedrs796052082
geneviewrs796052082
scholarrs796052082
googlers796052082
pharmgkbrs796052082
gwascentralrs796052082
openSNPrs796052082
23andMers796052082
23andMe allrs796052082
SNP Nexus

SNPshotrs796052082
SNPdbers796052082
MSV3drs796052082
GWAS Ctlgrs796052082
Max Magnitude
ClinVar
Risk rs796052082(;)
Alt rs796052082(;)
Reference rs796052082(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37430603delC
CLNSRC
CLNACC RCV000186460.1,