Have questions? Visit https://www.reddit.com/r/SNPedia

rs770050262

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs770050262(G;T)
Make rs770050262(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position97601990
GeneHOGA1
is asnp
is mentioned by
dbSNPrs770050262
ebirs770050262
HLIrs770050262
Exacrs770050262
Varsomers770050262
Maprs770050262
PheGenIrs770050262
hapmaprs770050262
1000 genomesrs770050262
hgdprs770050262
ensemblrs770050262
gopubmedrs770050262
geneviewrs770050262
scholarrs770050262
googlers770050262
pharmgkbrs770050262
gwascentralrs770050262
openSNPrs770050262
23andMers770050262
23andMe allrs770050262
SNP Nexus

SNPshotrs770050262
SNPdbers770050262
MSV3drs770050262
GWAS Ctlgrs770050262
Max Magnitude0
ClinVar
Risk rs770050262(A,T;A,T)
Alt rs770050262(A,T;A,T)
Reference rs770050262(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene HOGA1
CLNDBN Primary hyperoxaluria, type III
Reversed 0
HGVS NC_000010.10:g.99361747G>A
CLNSRC
CLNACC RCV000186493.1,