Original source

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

AG/- | MAF: 0.38 (-)

Chromosome 12:11688107-11688108 (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 2510 individual genotypes.

Variation displays