Original source

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

Alleles
-/A
Location

Chromosome 19: between 52188560 and 52188561 (forward strand) | View in location tab

Most severe consequence
HGVS name

19:g.52188560_52188561insA

About this variant

This variant overlaps 6 transcripts and has 1 individual genotype.

Variation displays