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rs149150736

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs149150736(C;T)
Make rs149150736(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position97611582
GeneHOGA1
is asnp
is mentioned by
dbSNPrs149150736
ebirs149150736
HLIrs149150736
Exacrs149150736
Varsomers149150736
Maprs149150736
PheGenIrs149150736
hapmaprs149150736
1000 genomesrs149150736
hgdprs149150736
ensemblrs149150736
gopubmedrs149150736
geneviewrs149150736
scholarrs149150736
googlers149150736
pharmgkbrs149150736
gwascentralrs149150736
openSNPrs149150736
23andMers149150736
23andMe allrs149150736
SNP Nexus

SNPshotrs149150736
SNPdbers149150736
MSV3drs149150736
GWAS Ctlgrs149150736
Max Magnitude0
ClinVar
Risk rs149150736(T;T)
Alt rs149150736(T;T)
Reference rs149150736(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene HOGA1
CLNDBN Primary hyperoxaluria, type III
Reversed 0
HGVS NC_000010.10:g.99371339C>T
CLNSRC
CLNACC RCV000186486.1,