Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.02 (T)

Chromosome 4:154565984 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status


Archive dbSNP rs57149658

HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 7 transcripts and has 2547 sample genotypes.

Variant displays