Original source

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

Alleles
C/- | Ancestral: C | MAF: < 0.01 (C)
Location

Chromosome 22:29281410 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 16 HGVS names - click the plus to show

About this variant

This variant overlaps 16 transcripts and has 2511 individual genotypes.

Variation displays