Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

A/G | Ancestral: A | Ambiguity code: R | MAF: 0.40 (A)

Chromosome 16:80995944 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs74248236

HGVS names

This variant has 23 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 23 transcripts and has 3688 sample genotypes.

Variant displays