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rs1057516292

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057516292(-;-)
Make rs1057516292(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position37429835
GeneGRHPR
is asnp
is mentioned by
dbSNPrs1057516292
dbSNP (old)rs1057516292
ClinGenrs1057516292
ebirs1057516292
HLIrs1057516292
Exacrs1057516292
Gnomadrs1057516292
Varsomers1057516292
Maprs1057516292
PheGenIrs1057516292
Biobankrs1057516292
1000 genomesrs1057516292
hgdprs1057516292
ensemblrs1057516292
gopubmedrs1057516292
geneviewrs1057516292
scholarrs1057516292
googlers1057516292
pharmgkbrs1057516292
gwascentralrs1057516292
openSNPrs1057516292
23andMers1057516292
23andMe allrs1057516292
SNPshotrs1057516292
SNPdbers1057516292
MSV3drs1057516292
GWAS Ctlgrs1057516292
Max Magnitude0
ClinVar
Risk rs1057516292(-;-)
Alt rs1057516292(-;-)
Reference Rs1057516292(T;T)
Significance Probable-Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37429832delT
CLNSRC
CLNACC RCV000409935.1,