Original source

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

Alleles
T/-|Ancestral: T
Location

Chromosome 5:68241387 (forward strand)|View in location tab

Co-located variant

dbSNP rs2545410 (T/G)

Most severe consequence
 
Intron variant
HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and 1 regulatory feature.

Variant displays