Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.19 (A)
Location

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

This variant has 11 HGVS names - click the plus to show

About this variant

This variant overlaps 23 transcripts and has 2588 sample genotypes.

Variant displays