Original source

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

Alleles
-/TTCG/TTTG | MAF: 0.41 (TTTG)
Location

Chromosome 8: between 23059514 and 23059515 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 2504 sample genotypes.

Variant displays