Original source

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

Alleles
AAAG/- | MAF: < 0.01 (-)
Location

Chromosome 6:57188572-57188575 (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