Original source

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

A/G | Ancestral: A | Ambiguity code: R | MAF: 0.07 (G)

Chromosome 16:89737297 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs17233847, rs12918188

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 23 transcripts and has 2584 sample genotypes.

Variant displays