Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.29 (G)
Location

Chromosome 16:74712505 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

16:g.74712505T>G

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 3691 individual genotypes.

Variation displays