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rs1057516299

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057516299(-;-)
Make rs1057516299(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position37426654
GeneGRHPR
is asnp
is mentioned by
dbSNPrs1057516299
dbSNP (classic)rs1057516299
ClinGenrs1057516299
ebirs1057516299
HLIrs1057516299
Exacrs1057516299
Gnomadrs1057516299
Varsomers1057516299
LitVarrs1057516299
Maprs1057516299
PheGenIrs1057516299
Biobankrs1057516299
1000 genomesrs1057516299
hgdprs1057516299
ensemblrs1057516299
geneviewrs1057516299
scholarrs1057516299
googlers1057516299
pharmgkbrs1057516299
gwascentralrs1057516299
openSNPrs1057516299
23andMers1057516299
23andMe allrs1057516299
SNPshotrs1057516299
SNPdbers1057516299
MSV3drs1057516299
GWAS Ctlgrs1057516299
Max Magnitude0
ClinVar
Risk rs1057516299(-;-)
Alt rs1057516299(-;-)
Reference Rs1057516299(A;A)
Significance Probable-Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37426651delA
CLNSRC
CLNACC RCV000410867.1,