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rs1057517238

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057517238(-;A)
Make rs1057517238(A;A)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position37425935
GeneGRHPR
is asnp
is mentioned by
dbSNPrs1057517238
dbSNP (old)rs1057517238
ClinGenrs1057517238
ebirs1057517238
HLIrs1057517238
Exacrs1057517238
Gnomadrs1057517238
Varsomers1057517238
Maprs1057517238
PheGenIrs1057517238
Biobankrs1057517238
1000 genomesrs1057517238
hgdprs1057517238
ensemblrs1057517238
gopubmedrs1057517238
geneviewrs1057517238
scholarrs1057517238
googlers1057517238
pharmgkbrs1057517238
gwascentralrs1057517238
openSNPrs1057517238
23andMers1057517238
23andMe allrs1057517238
SNPshotrs1057517238
SNPdbers1057517238
MSV3drs1057517238
GWAS Ctlgrs1057517238
Max Magnitude0
ClinVar
Risk rs1057517238(A;A)
Alt rs1057517238(A;A)
Reference Rs1057517238(-;-)
Significance Probable-Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37425932dupA
CLNSRC
CLNACC RCV000411412.1,