Original source

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

Alleles
T/G|Ancestral: T|Ambiguity code: K|MAF: 0.01 (G)
Location

Chromosome 1:116908708 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

1:g.116908708T>G

About this variant

This variant overlaps 3 transcripts and has 2504 sample genotypes.

Variant displays