Original source

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

Alleles
TTT/-
Location

Chromosome 10:112957214-112957216 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Synonyms

Archive dbSNP rs57636197, rs72192370

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 15 transcripts.

Variant displays