Original source

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


Chromosome 10: between 99531107 and 99531108 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and 1 regulatory feature.

Variant displays