Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K
Location

Chromosome 1:27013891 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

1:g.27013891G>T

About this variant

This variant overlaps 1 transcript.

Variant displays