Original source

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

Alleles
-/G
Location

Chromosome 5: between 132869136 and 132869137 (forward strand) | View in location tab

Most severe consequence
HGVS name

5:g.132869136_132869137insG

About this variant

This variant overlaps 16 transcripts.

Variation displays