Original source

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

Alleles
A/- | Ancestral: A
Location

Chromosome 10:68987043 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

10:g.68987043delA

About this variant

This variant overlaps 6 transcripts and has 1 individual genotype.

Variation displays