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rs1057517398

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517398(G;G)
Make rs1057517398(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position37424977
GeneGRHPR
is asnp
is mentioned by
dbSNPrs1057517398
dbSNP (old)rs1057517398
ClinGenrs1057517398
ebirs1057517398
HLIrs1057517398
Exacrs1057517398
Gnomadrs1057517398
Varsomers1057517398
Maprs1057517398
PheGenIrs1057517398
Biobankrs1057517398
1000 genomesrs1057517398
hgdprs1057517398
ensemblrs1057517398
gopubmedrs1057517398
geneviewrs1057517398
scholarrs1057517398
googlers1057517398
pharmgkbrs1057517398
gwascentralrs1057517398
openSNPrs1057517398
23andMers1057517398
23andMe allrs1057517398
SNPshotrs1057517398
SNPdbers1057517398
MSV3drs1057517398
GWAS Ctlgrs1057517398
Max Magnitude0
ClinVar
Risk rs1057517398(G;G)
Alt rs1057517398(G;G)
Reference Rs1057517398(T;T)
Significance Probable-Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37424974T>G
CLNSRC
CLNACC RCV000410412.1,