Original source

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

Alleles
C/- | Ancestral: C | MAF: 0.11 (-)
Location

Chromosome 12:132634660 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and has 2590 individual genotypes.

Variation displays