Original source

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

Alleles
A/-|Ancestral: A
Location

Chromosome 16:74720167 (forward strand)|View in location tab

Co-located variant

dbSNP rs74250246 (A/T)

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 4 transcripts.

Variant displays