Original source

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

C/A/T | Ancestral: C | Ambiguity code: H | MAF: 0.01 (T)

Chromosome 16:3596179 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Archive dbSNP rs3169471

HGVS names

This variant has 14 HGVS names - Show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 8 transcripts and has 2504 sample genotypes.

Variant displays