Original source

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

GT/- | MAF: 0.33 (-)

Chromosome 3:128752126-128752127 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs146095027, rs142981000

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

About this variant

This variant overlaps 5 transcripts and has 2507 individual genotypes.

Variation displays