Original source

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

Alleles
-/T | MAF: 0.25 (-)
Location

Chromosome 3: between 129062415 and 129062416 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

3:g.129062415_129062416insT

About this variant

This variant overlaps 2 transcripts and has 2504 individual genotypes.

Variation displays