Original source

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

Alleles
-/C/G/TTG/TTGTGTG
Location

Chromosome 10: between 119665092 and 119665093 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 20 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and 1 regulatory feature.

Variant displays