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rs138207257

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs138207257(G;T)
Make rs138207257(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position97611535
GeneHOGA1
is asnp
is mentioned by
dbSNPrs138207257
ebirs138207257
HLIrs138207257
Exacrs138207257
Varsomers138207257
Maprs138207257
PheGenIrs138207257
hapmaprs138207257
1000 genomesrs138207257
hgdprs138207257
ensemblrs138207257
gopubmedrs138207257
geneviewrs138207257
scholarrs138207257
googlers138207257
pharmgkbrs138207257
gwascentralrs138207257
openSNPrs138207257
23andMers138207257
23andMe allrs138207257
SNP Nexus

SNPshotrs138207257
SNPdbers138207257
MSV3drs138207257
GWAS Ctlgrs138207257
Max Magnitude0
ClinVar
Risk rs138207257(A,T;A,T)
Alt rs138207257(A,T;A,T)
Reference rs138207257(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene HOGA1
CLNDBN Primary hyperoxaluria, type III
Reversed 0
HGVS NC_000010.10:g.99371292G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000047.2,