Original source

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

Alleles
-/A
Location

Chromosome 11: between 119184540 and 119184541 (forward strand) | View in location tab

Most severe consequence
HGVS name

11:g.119184540_119184541insA

About this variant

This variant overlaps 21 transcripts.

Variation displays