Original source

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

Alleles
A/C/T | Ancestral: T | Ambiguity code: H | MAF: 0.18 (A)
Location

Chromosome 6:1613294 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 4 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2572 individual genotypes.

Variation displays