Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.41 (A)
Location

Chromosome 17:18365454 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms
HGVS name

17:g.18365454A>G

About this variant

This variant overlaps 8 transcripts and has 2510 sample genotypes.

Variant displays