Original source

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

Alleles
-/CTCT|MAF: 0.45 (CTCT)
Location

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