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 4:120706092 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 6 transcripts.

Variant displays