Original source

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

Alleles
-/A|MAF: 0.21 (A)
Location

Chromosome 13: between 27919351 and 27919352 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and has 2509 sample genotypes.

Variant displays