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rs150702945

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs150702945(C;C)
Make rs150702945(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position97598900
GeneHOGA1
is asnp
is mentioned by
dbSNPrs150702945
dbSNP (classic)rs150702945
ClinGenrs150702945
ebirs150702945
HLIrs150702945
Exacrs150702945
Gnomadrs150702945
Varsomers150702945
LitVarrs150702945
Maprs150702945
PheGenIrs150702945
Biobankrs150702945
1000 genomesrs150702945
hgdprs150702945
ensemblrs150702945
geneviewrs150702945
scholarrs150702945
googlers150702945
pharmgkbrs150702945
gwascentralrs150702945
openSNPrs150702945
23andMers150702945
SNPshotrs150702945
SNPdbers150702945
MSV3drs150702945
GWAS Ctlgrs150702945
Max Magnitude0
ClinVar
Risk rs150702945(A;A) rs150702945(C;C)
Alt rs150702945(A;A) rs150702945(C;C)
Reference Rs150702945(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene HOGA1
CLNDBN Primary hyperoxaluria, type III
Reversed 0
HGVS NC_000010.10:g.99358657G>A
CLNSRC
CLNACC RCV000186477.1,