Original source

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


Chromosome 19: between 51903028 and 51903029 (forward strand) | View in location tab

Most severe consequence
Intron variant
HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 8 transcripts.

Variant displays