Original source

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

Alleles
-/C
Location

Chromosome 18: between 903131 and 903132 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 9 transcripts.

Variant displays