Original source

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

T/G | Ancestral: T | Ambiguity code: K | MAF: < 0.01 (G)

Chromosome 16:23635127 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


LSDB NM_024675.3:c.1419A>C

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 6 transcripts, has 2504 sample genotypes, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays