Original source

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

Alleles
A/- | Ancestral: A
Location

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

Co-located

with dbSNP rs74250246 (A/T)

Most severe consequence
 
Intron variant

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts.

Variant displays