Original source

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

T/C/G | Ancestral: G | Ambiguity code: B | MAF: 0.01 (G)

Chromosome 16:88809520 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Archive dbSNP rs117055399, rs3167705

HGVS names

This variant has 20 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 36 transcripts and has 2597 sample genotypes.

Variant displays