Original source

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

-/CTCT | MAF: 0.45 (CTCT)

Chromosome 5: between 148097110 and 148097111 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and has 2504 sample genotypes.

Variant displays