Original source

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

T/A | Ancestral: T | Ambiguity code: W | MAF: 0.31 (T)

Chromosome 14:100342173 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 13 transcripts and has 2688 sample genotypes.

Variant displays