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rs672601351

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs672601351(-;-)
Make rs672601351(-;TG)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position37425955
GeneGRHPR
is asnp
is mentioned by
dbSNPrs672601351
ebirs672601351
HLIrs672601351
Exacrs672601351
Varsomers672601351
Maprs672601351
PheGenIrs672601351
hapmaprs672601351
1000 genomesrs672601351
hgdprs672601351
ensemblrs672601351
gopubmedrs672601351
geneviewrs672601351
scholarrs672601351
googlers672601351
pharmgkbrs672601351
gwascentralrs672601351
openSNPrs672601351
23andMers672601351
23andMe allrs672601351
SNP Nexus

SNPshotrs672601351
SNPdbers672601351
MSV3drs672601351
GWAS Ctlgrs672601351
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs672601351(TG;TG)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37425952_37425953delTG
CLNSRC OMIM Allelic Variant
CLNACC RCV000149442.5,