Original source

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

Alleles
-/C/G
Location

Chromosome 20: between 58652376 and 58652377 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 44 HGVS names - Show

About this variant

This variant overlaps 42 transcripts and 1 regulatory feature.

Variant displays