Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

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

Co-located variant

dbSNP rs559798767 (T/A)

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 15 transcripts and has 2508 sample genotypes.

Variant displays