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rs376844297

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs376844297(A;A)
Make rs376844297(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position240869356
GeneAGXT, LOC105373969
is asnp
is mentioned by
dbSNPrs376844297
ebirs376844297
HLIrs376844297
Exacrs376844297
Varsomers376844297
Maprs376844297
PheGenIrs376844297
hapmaprs376844297
1000 genomesrs376844297
hgdprs376844297
ensemblrs376844297
gopubmedrs376844297
geneviewrs376844297
scholarrs376844297
googlers376844297
pharmgkbrs376844297
gwascentralrs376844297
openSNPrs376844297
23andMers376844297
23andMe allrs376844297
SNP Nexus

SNPshotrs376844297
SNPdbers376844297
MSV3drs376844297
GWAS Ctlgrs376844297
Max Magnitude0
ClinVar
Risk rs376844297(A,T;A,T)
Alt rs376844297(A,T;A,T)
Reference rs376844297(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808773C>T
CLNSRC
CLNACC RCV000186301.1,