Original source

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

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: 0.06 (G)
Location

Chromosome 13:33015717 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

13:g.33015717T>G

About this variant

This variant overlaps 2 transcripts and has 2505 sample genotypes.

Variant displays