Original source

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

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

Chromosome 19:55158331 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 27 transcripts and has 2 sample genotypes.

Variant displays