Original source

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

Alleles
-/TATG | MAF: 0.48 (TATG)
Location

Chromosome 12: between 20833891 and 20833892 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 2504 individual genotypes.

Variation displays