Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.18 (A)

Chromosome 16:74747619 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs918749, rs74250248

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 2 transcripts and has 2512 sample genotypes.

Variant displays