Original source

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

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.43 (C)

Chromosome 16:2299370 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs1637592

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 3 transcripts, has 2558 sample genotypes and is mentioned in 2 citations.

Variant displays