Original source

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

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

Chromosome 4:73982129 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

4:g.73982129C>T

About this variant

Variant displays