Original source

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

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

Chromosome 4:74037449 (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