Original source

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

Alleles
-/G
Location

Chromosome 11: between 636087 and 636088 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

11:g.636087_636088insG

About this variant

This variant overlaps 2 transcripts and has 7 individual genotypes.

Variation displays