Original source

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

Alleles
-/T
Location

Chromosome 3: between 128752738 and 128752739 (forward strand) | View in location tab

Most severe consequence
 
Intron variant

This variant has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 1 sample genotype.

Variant displays