Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.48 (G)
Location

Chromosome 3:184378790 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR084015

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57526857, rs386619456

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

This variation has assays on 8 chips - click the plus to show

About this variant

This variant overlaps 21 transcripts, has 2663 individual genotypes and is mentioned in 1 citation.

Variation displays