Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.43 (T)

Chromosome 1:231395881 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs56654310

This variation has 3 HGVS names - click the plus to show

This variation has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts, has 3762 individual genotypes and is mentioned in 6 citations.

Variation displays