Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

C/- | Ancestral: C

Chromosome 19:40749405 (forward strand) | View in location tab

Most severe consequence
Intron variant

This variant has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 18 transcripts.

Variant displays