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rs1057516823

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057516823(-;A)
Make rs1057516823(A;A)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position37432028
GeneGRHPR
is asnp
is mentioned by
dbSNPrs1057516823
dbSNP (old)rs1057516823
ClinGenrs1057516823
ebirs1057516823
HLIrs1057516823
Exacrs1057516823
Gnomadrs1057516823
Varsomers1057516823
Maprs1057516823
PheGenIrs1057516823
Biobankrs1057516823
1000 genomesrs1057516823
hgdprs1057516823
ensemblrs1057516823
gopubmedrs1057516823
geneviewrs1057516823
scholarrs1057516823
googlers1057516823
pharmgkbrs1057516823
gwascentralrs1057516823
openSNPrs1057516823
23andMers1057516823
23andMe allrs1057516823
SNPshotrs1057516823
SNPdbers1057516823
MSV3drs1057516823
GWAS Ctlgrs1057516823
Max Magnitude0
ClinVar
Risk rs1057516823(A;A)
Alt rs1057516823(A;A)
Reference Rs1057516823(-;-)
Significance Probable-Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37432025dupA
CLNSRC
CLNACC RCV000409413.1,