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rs876661297

From SNPedia

Orientationplus
Geno Mag Summary
(AGA;AGA) 0 common in clinvar
Make rs876661297(-;-)
Make rs876661297(-;AAG)
Make rs876661297(AAG;AAG)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position3129168
GeneTRNT1
is asnp
is mentioned by
dbSNPrs876661297
ebirs876661297
HLIrs876661297
Exacrs876661297
Varsomers876661297
Maprs876661297
PheGenIrs876661297
hapmaprs876661297
1000 genomesrs876661297
hgdprs876661297
ensemblrs876661297
gopubmedrs876661297
geneviewrs876661297
scholarrs876661297
googlers876661297
pharmgkbrs876661297
gwascentralrs876661297
openSNPrs876661297
23andMers876661297
23andMe allrs876661297
SNP Nexus

SNPshotrs876661297
SNPdbers876661297
MSV3drs876661297
GWAS Ctlgrs876661297
Max Magnitude0
ClinVar
Risk rs876661297(;)
Alt rs876661297(;)
Reference rs876661297(AGA;AGA)
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.3170852_3170854delAAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000223678.1,