Original source

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

Alleles
AAAG/- | MAF: 0.16 (-)
Location

Chromosome 11:114079111-114079114 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 2505 individual genotypes.

Variation displays