Original source

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

C/T | Ancestral: C | Ambiguity code: Y

Chromosome 19:42326117 (forward strand) | View in location tab

Most severe consequence
5 prime UTR variant
Evidence status

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and 1 regulatory feature.

Variant displays