Original source

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

Alleles
-/T
Location

Chromosome 6: between 32635411 and 32635412 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 7 transcripts.

Variant displays