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rs876661299

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876661299(C;C)
Make rs876661299(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position3146404
GeneTRNT1
is asnp
is mentioned by
dbSNPrs876661299
ebirs876661299
HLIrs876661299
Exacrs876661299
Varsomers876661299
Maprs876661299
PheGenIrs876661299
hapmaprs876661299
1000 genomesrs876661299
hgdprs876661299
ensemblrs876661299
gopubmedrs876661299
geneviewrs876661299
scholarrs876661299
googlers876661299
pharmgkbrs876661299
gwascentralrs876661299
openSNPrs876661299
23andMers876661299
23andMe allrs876661299
SNP Nexus

SNPshotrs876661299
SNPdbers876661299
MSV3drs876661299
GWAS Ctlgrs876661299
Max Magnitude0
ClinVar
Risk rs876661299(C;C)
Alt rs876661299(C;C)
Reference rs876661299(T;T)
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.3188088T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000223676.1,