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rs201803986

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201803986(C;T)
Make rs201803986(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position97584810
GeneHOGA1
is asnp
is mentioned by
dbSNPrs201803986
ebirs201803986
HLIrs201803986
Exacrs201803986
Varsomers201803986
Maprs201803986
PheGenIrs201803986
hapmaprs201803986
1000 genomesrs201803986
hgdprs201803986
ensemblrs201803986
gopubmedrs201803986
geneviewrs201803986
scholarrs201803986
googlers201803986
pharmgkbrs201803986
gwascentralrs201803986
openSNPrs201803986
23andMers201803986
23andMe allrs201803986
SNP Nexus

SNPshotrs201803986
SNPdbers201803986
MSV3drs201803986
GWAS Ctlgrs201803986
Max Magnitude0
ClinVar
Risk rs201803986(A,T;A,T)
Alt rs201803986(A,T;A,T)
Reference rs201803986(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene HOGA1
CLNDBN Primary hyperoxaluria, type III
Reversed 0
HGVS NC_000010.10:g.99344567C>T
CLNSRC
CLNACC RCV000186472.1,