Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17227163

This variant has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 14 transcripts and has 2594 sample genotypes.

Variant displays