Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K|MAF: 0.11 (T)
Location

Chromosome 16:108663 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57802088, rs798611

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2505 sample genotypes.

Variant displays