Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.04 (G)
Location

Chromosome 5:161845429 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

5:g.161845429A>G

About this variant

This variant overlaps 6 transcripts and has 2505 sample genotypes.

Variant displays