Original source

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

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.24 (T)

Chromosome 7:155461450 (forward strand) | View in location tab


with HGMD-PUBLIC CS045644

Most severe consequence
Intron variant
Evidence status

Clinical significance


Archive dbSNP rs3808333

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 2 transcripts, has 3520 sample genotypes, is associated with 3 phenotypes and is mentioned in 13 citations.

Variant displays