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rs1057517026

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs1057517026(-;-)
Make rs1057517026(-;TG)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position37428520
GeneGRHPR
is asnp
is mentioned by
dbSNPrs1057517026
dbSNP (old)rs1057517026
ClinGenrs1057517026
ebirs1057517026
HLIrs1057517026
Exacrs1057517026
Gnomadrs1057517026
Varsomers1057517026
LitVarrs1057517026
Maprs1057517026
PheGenIrs1057517026
Biobankrs1057517026
1000 genomesrs1057517026
hgdprs1057517026
ensemblrs1057517026
gopubmedrs1057517026
geneviewrs1057517026
scholarrs1057517026
googlers1057517026
pharmgkbrs1057517026
gwascentralrs1057517026
openSNPrs1057517026
23andMers1057517026
23andMe allrs1057517026
SNPshotrs1057517026
SNPdbers1057517026
MSV3drs1057517026
GWAS Ctlgrs1057517026
Max Magnitude0
ClinVar
Risk rs1057517026(-;-)
Alt rs1057517026(-;-)
Reference Rs1057517026(TG;TG)
Significance Probable-Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37428517_37428518delTG
CLNSRC
CLNACC RCV000411789.1,