Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.45 (C)
Location

Chromosome 6:160716747 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

This variation has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 6 transcripts, has 2549 individual genotypes, is associated with 1 phenotype and is mentioned in 3 citations.

Variation displays