Original source

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

Alleles
C/A/G/T | Ancestral: C | Ambiguity code: N
Location

Chromosome 11:1996229 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 39 HGVS names - click the plus to show

About this variant

This variant overlaps 54 transcripts.

Variant displays