Original source

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

Alleles
T/- | Ancestral: T | MAF: 0.41 (-)
Location

Chromosome 22:29283695 (forward strand) | View in location tab

Co-located

with dbSNP rs559798767 (T/A)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

This variant has 14 HGVS names - click the plus to show

About this variant

This variant overlaps 15 transcripts and has 2508 sample genotypes.

Variant displays