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rs876661298

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876661298(-;-)
Make rs876661298(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position3148101
GeneTRNT1
is asnp
is mentioned by
dbSNPrs876661298
ebirs876661298
HLIrs876661298
Exacrs876661298
Varsomers876661298
Maprs876661298
PheGenIrs876661298
hapmaprs876661298
1000 genomesrs876661298
hgdprs876661298
ensemblrs876661298
gopubmedrs876661298
geneviewrs876661298
scholarrs876661298
googlers876661298
pharmgkbrs876661298
gwascentralrs876661298
openSNPrs876661298
23andMers876661298
23andMe allrs876661298
SNP Nexus

SNPshotrs876661298
SNPdbers876661298
MSV3drs876661298
GWAS Ctlgrs876661298
Max Magnitude0
ClinVar
Risk rs876661298(;)
Alt rs876661298(;)
Reference rs876661298(A;A)
Significance Pathogenic
Disease Retinitis pigmentosa and erythrocytic microcytosis
Variation info
Gene TRNT1
CLNDBN Retinitis pigmentosa and erythrocytic microcytosis
Reversed 0
HGVS NC_000003.11:g.3189785delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000223667.1,