Original source

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

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

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


with HGMD-PUBLIC CR084015

Most severe consequence
Evidence status


Archive dbSNP rs57526857

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 2398 individual genotypes and is mentioned in 1 citation.

Variation displays