Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.41 (C)
Location

Chromosome 4:88074643 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61246840

This variation has 6 HGVS names - click the plus to show

This variation has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 3751 individual genotypes.

Variation displays