Original source

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

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

Chromosome 4:74037448 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature and has 1 sample genotype.

Variant displays