Original source

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

Alleles
-/C
Location

Chromosome 13: between 23199744 and 23199745 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 2 transcripts.

Variant displays