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 2:219251670 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 17 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 25 transcripts and has 2599 sample genotypes.

Variant displays