Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.25 (C)
Location

Chromosome 19:8959216 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 4 synonyms - click the plus to show

This variation has 3 HGVS names - click the plus to show

This variation has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 1 transcript and has 3692 individual genotypes.

Variation displays