Original source

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

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

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