Original source

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

T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.34 (C)

Chromosome 18:55228300 (forward strand)|View in location tab

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


Archive dbSNP rs1049450, rs6567211, rs3189620

HGVS names

This variant has 55 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 28 transcripts, 1 regulatory feature, has 2542 sample genotypes and is associated with 1 phenotype.

Variant displays