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rs878853266

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853266(-;-)
Make rs878853266(-;A)
Make rs878853266(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position3148101
GeneTRNT1
is asnp
is mentioned by
dbSNPrs878853266
ebirs878853266
HLIrs878853266
Exacrs878853266
Varsomers878853266
Maprs878853266
PheGenIrs878853266
hapmaprs878853266
1000 genomesrs878853266
hgdprs878853266
ensemblrs878853266
gopubmedrs878853266
geneviewrs878853266
scholarrs878853266
googlers878853266
pharmgkbrs878853266
gwascentralrs878853266
openSNPrs878853266
23andMers878853266
23andMe allrs878853266
SNP Nexus

SNPshotrs878853266
SNPdbers878853266
MSV3drs878853266
GWAS Ctlgrs878853266
Max Magnitude0
ClinVar
Risk rs878853266(A;A)
Alt rs878853266(A;A)
Reference rs878853266(;)
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.3189785dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000223673.1,