Original source

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

-/TG | MAF: 0.24 (TG)

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

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and has 2504 sample genotypes.

Variant displays