Original source

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

Alleles
TTTT/-
Location

Chromosome 10:6188850-6188853 (forward strand)|View in location tab

Co-located variant

dbSNP rs141745788 (TTTT/-)

Most severe consequence
 
Intron variant
Synonyms

Archive dbSNP rs60895048

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and 1 regulatory feature.

Variant displays