Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.44 (T)
Location

Chromosome 16:2278649 (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 6 chips - click the plus to show

About this variant

This variant overlaps 6 transcripts, has 2396 individual genotypes and is mentioned in 2 citations.

Variation displays