Original source

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

-/AA/CA | MAF: 0.45 (-)

Chromosome 11: between 102578792 and 102578793 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2504 sample genotypes.

Variant displays