Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.18 (C)
Location

Chromosome 4:6280234 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs386611056, rs57851868

This variation has 4 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 3 transcripts, has 3615 individual genotypes and is mentioned in 5 citations.

Variation displays