Original source

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

Alleles
CACT/-|MAF: 0.01 (-)
Location

Chromosome 19:48968172-48968175 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 2504 sample genotypes.

Variant displays