Original source

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

Alleles
G/- | Ancestral: G
Location

Chromosome 11:27700541 (forward strand) | View in location tab

Most severe consequence

This variation has 14 HGVS names - click the plus to show

About this variant

This variant overlaps 22 transcripts.

Variation displays