Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.04 (C)
Location

Chromosome 3:15479331 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs386610770, rs56528226

This variation has 7 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 7 transcripts, has 2645 individual genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variation displays