Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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

Co-located

with dbSNP rs71591574 (C/TT)

Most severe consequence
 
Intron variant

This variant has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts.

Variant displays