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
Evidence status

Synonyms

Archive dbSNP rs147271649

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

About this variant

This variant overlaps 8 transcripts and has 2506 individual genotypes.

Variation displays