Original source

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

Alleles
AAAAAAAAAAAA/- | MAF: 0.02 (AAAAAAAAAAAA)
Location

Chromosome 7:101132725-101132736 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript and has 2505 individual genotypes.

Variation displays