Original source

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

CT/- | MAF: 0.42 (-)

Chromosome 4:41746722-41746723 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 2508 sample genotypes.

Variant displays