Original source

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

Alleles
C/-|Ancestral: C|MAF: 0.29 (C)
Location

Chromosome 11:62701080 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 19 transcripts and has 2512 sample genotypes.

Variant displays