Original source

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

T/C | Ambiguity code: Y | MAF: 0.46 (C)

Chromosome 16:28478025 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 28 HGVS names - Show

About this variant

This variant overlaps 35 transcripts and has 2510 sample genotypes.

Variant displays