Original source

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

Alleles
T/-|MAF: < 0.01 (T)
Location

Chromosome 22:29275069 (forward strand)|View in location tab

Co-located variant

dbSNP rs199834978 (T/C)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs33914653, rs60449778

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 18 transcripts and has 2516 sample genotypes.

Variant displays