Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
CTC/- | MAF: 0.08 (-)
Location

Chromosome 13:27644768-27644770 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs147271649

This variant has 7 HGVS names - click the plus to show

About this variant

Variant displays