Original source

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

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

Chromosome 4:73982146 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

4:g.73982146C>T

About this variant

Variant displays