Original source

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

Alleles
AA/-
Location

Chromosome 11:114146865-114146866 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60625868, rs71063550

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts.

Variant displays