Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.29 (A)
Location

Chromosome 22:50628493 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

22:g.50628493G>A

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 3780 individual genotypes.

Variation displays