Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.22 (T)

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


with HGMD-PUBLIC CS045644

Most severe consequence
Evidence status

Clinical significance


Archive dbSNP rs3808333

This variation has 2 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 2126 individual genotypes, is associated with 3 phenotypes and is mentioned in 12 citations.

Variation displays