Original source

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

Alleles
-/T | MAF: 0.44 (-)
Location

Chromosome 6: between 34426907 and 34426908 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

6:g.34426907_34426908insT

About this variant

This variant overlaps 8 transcripts and has 2508 individual genotypes.

Variation displays