Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.17 (G)
Location

Chromosome 1:20632353 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

1:g.20632353A>G

About this variant

This variant overlaps 2 transcripts and has 2508 sample genotypes.

Variant displays