Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 22 HGVS names - Show

About this variant

This variant overlaps 46 transcripts and has 2588 sample genotypes.

Variant displays