Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.11 (T)

Chromosome 16:50743391 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs57304152

HGVS names

This variant has 13 HGVS names - Show

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 14 transcripts, 1 regulatory feature, has 3723 sample genotypes and is mentioned in 1 citation.

Variant displays