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rs1057516941

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057516941(-;A)
Make rs1057516941(A;A)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position37428533
GeneGRHPR
is asnp
is mentioned by
dbSNPrs1057516941
dbSNP (old)rs1057516941
ClinGenrs1057516941
ebirs1057516941
HLIrs1057516941
Exacrs1057516941
Gnomadrs1057516941
Varsomers1057516941
LitVarrs1057516941
Maprs1057516941
PheGenIrs1057516941
Biobankrs1057516941
1000 genomesrs1057516941
hgdprs1057516941
ensemblrs1057516941
gopubmedrs1057516941
geneviewrs1057516941
scholarrs1057516941
googlers1057516941
pharmgkbrs1057516941
gwascentralrs1057516941
openSNPrs1057516941
23andMers1057516941
23andMe allrs1057516941
SNPshotrs1057516941
SNPdbers1057516941
MSV3drs1057516941
GWAS Ctlgrs1057516941
Max Magnitude0
ClinVar
Risk rs1057516941(A;A)
Alt rs1057516941(A;A)
Reference Rs1057516941(-;-)
Significance Probable-Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37428530dupA
CLNSRC
CLNACC RCV000411634.1,