Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.27 (G)
Location

Chromosome 8:96160175 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

About this variant

This variant overlaps 4 transcripts and has 2506 individual genotypes.

Variation displays