Original source

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

Alleles
A/- | Ancestral: A
Location

Chromosome 7:100720172 (forward strand) | View in location tab

Most severe consequence
HGVS name

7:g.100720172delA

About this variant

This variant overlaps 2 transcripts and has 3 individual genotypes.

Variation displays