Original source

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

-/TGTT | MAF: 0.01 (TGTT)

Chromosome 6: between 57188636 and 57188637 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2504 individual genotypes.

Variation displays