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

rs878853351

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853351(A;A)
Make rs878853351(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position154744799
GeneLRAT
is asnp
is mentioned by
dbSNPrs878853351
ebirs878853351
HLIrs878853351
Exacrs878853351
Varsomers878853351
Maprs878853351
PheGenIrs878853351
hapmaprs878853351
1000 genomesrs878853351
hgdprs878853351
ensemblrs878853351
gopubmedrs878853351
geneviewrs878853351
scholarrs878853351
googlers878853351
pharmgkbrs878853351
gwascentralrs878853351
openSNPrs878853351
23andMers878853351
23andMe allrs878853351
SNP Nexus

SNPshotrs878853351
SNPdbers878853351
MSV3drs878853351
GWAS Ctlgrs878853351
Max Magnitude0
ClinVar
Risk rs878853351(A;A)
Alt rs878853351(A;A)
Reference rs878853351(G;G)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene LRAT
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000004.11:g.155665951G>A
CLNSRC
CLNACC RCV000225673.1,