Original source

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

Alleles
G/-|Ancestral: T
Location

Chromosome 10:119662226 (forward strand)|View in location tab

Co-located variant

dbSNP rs2736423 (G/T)

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 3 transcripts.

Variant displays