Original source

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

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

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

Co-located

with dbSNP rs199834978 (T/C)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60449778, rs33914653

This variant has 16 HGVS names - click the plus to show

About this variant

This variant overlaps 18 transcripts and has 2516 sample genotypes.

Variant displays