Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
Evidence status

Synonyms

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 2509 individual genotypes.

Variation displays