Original source

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

Alleles
TG/-|MAF: 0.01 (-)
Location

Chromosome 20:23633487-23633488 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2504 sample genotypes.

Variant displays