Original source

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

-/C | MAF: 0.25 (-)

Chromosome 18: between 5437962 and 5437963 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 2517 sample genotypes.

Variant displays