Original source

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

T/G | Ancestral: G | Ambiguity code: K | MAF: 0.25 (G)

Chromosome 16:89747558 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs17227163

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 14 transcripts and has 2594 sample genotypes.

Variant displays