Original source

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

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.12 (T)

Chromosome 5:161888763 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs57223367

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 5 transcripts and has 3141 sample genotypes.

Variant displays