Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057516831

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057516831(-;-)
Make rs1057516831(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position37436749
GeneGRHPR
is asnp
is mentioned by
dbSNPrs1057516831
dbSNP (old)rs1057516831
ClinGenrs1057516831
ebirs1057516831
HLIrs1057516831
Exacrs1057516831
Gnomadrs1057516831
Varsomers1057516831
Maprs1057516831
PheGenIrs1057516831
Biobankrs1057516831
1000 genomesrs1057516831
hgdprs1057516831
ensemblrs1057516831
gopubmedrs1057516831
geneviewrs1057516831
scholarrs1057516831
googlers1057516831
pharmgkbrs1057516831
gwascentralrs1057516831
openSNPrs1057516831
23andMers1057516831
23andMe allrs1057516831
SNPshotrs1057516831
SNPdbers1057516831
MSV3drs1057516831
GWAS Ctlgrs1057516831
Max Magnitude0
ClinVar
Risk rs1057516831(-;-)
Alt rs1057516831(-;-)
Reference Rs1057516831(A;A)
Significance Probable-Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37436746delA
CLNSRC
CLNACC RCV000409992.1,