Original source

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

A/C/G | Ancestral: G | Ambiguity code: V | MAF: 0.19 (A)

Chromosome 16:89737262 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 22 HGVS names - Show

About this variant

This variant overlaps 46 transcripts and has 2588 sample genotypes.

Variant displays