Original source

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

Alleles
TTTT/-
Location

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

Most severe consequence
 
Intron variant
Synonyms

Archive dbSNP rs60895048

This variant has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts and 1 regulatory feature.

Variant displays