Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

G/- | Ancestral: G

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

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 21 transcripts and 1 regulatory feature.

Variant displays