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rs767405535

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs767405535(C;T)
Make rs767405535(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position97599094
GeneHOGA1
is asnp
is mentioned by
dbSNPrs767405535
ebirs767405535
HLIrs767405535
Exacrs767405535
Varsomers767405535
Maprs767405535
PheGenIrs767405535
hapmaprs767405535
1000 genomesrs767405535
hgdprs767405535
ensemblrs767405535
gopubmedrs767405535
geneviewrs767405535
scholarrs767405535
googlers767405535
pharmgkbrs767405535
gwascentralrs767405535
openSNPrs767405535
23andMers767405535
23andMe allrs767405535
SNP Nexus

SNPshotrs767405535
SNPdbers767405535
MSV3drs767405535
GWAS Ctlgrs767405535
Max Magnitude0
ClinVar
Risk rs767405535(A,T;A,T)
Alt rs767405535(A,T;A,T)
Reference rs767405535(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene HOGA1
CLNDBN Primary hyperoxaluria, type III
Reversed 0
HGVS NC_000010.10:g.99358851C>T
CLNSRC
CLNACC RCV000186478.1,