Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W
Location

Chromosome 6:143995144 (forward strand) | View in location tab

Most severe consequence
 
Intron variant

This variant has 19 HGVS names - click the plus to show

About this variant

This variant overlaps 18 transcripts.

Variant displays