Original source

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

A/C | Ancestral: A | Ambiguity code: M

Chromosome 11:1995992 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 18 transcripts and has 253 sample genotypes.

Variant displays