Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.03 (A)
Location

Chromosome 22:50569993 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts and has 2505 individual genotypes.

Variation displays