Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.36 (A)
Location

Chromosome 6:111222741 (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 4 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 2508 individual genotypes and is mentioned in 2 citations.

Variation displays