Original source

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

Alleles
-/TG | MAF: 0.24 (TG)
Location

Chromosome 13: between 23195678 and 23195679 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 2504 sample genotypes.

Variant displays