Original source

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

Alleles
T/- | Ancestral: T | MAF: 0.20 (T)
Location

Chromosome 22:40344578 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

22:g.40344578delT

About this variant

This variant overlaps 10 transcripts and has 2509 individual genotypes.

Variation displays