Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.01 (T)

Chromosome 1:201365603 (forward strand) | View in location tab

Most severe consequence
Splice region variant
Evidence status

Clinical significance


LSDB TNNT2_264+7G_A_071811

HGVS names

This variant has 19 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 25 transcripts, has 2504 sample genotypes, is associated with 2 phenotypes and is mentioned in 2 citations.

Variant displays