Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 18:5392524 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3204776, rs386518158

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

Genotyping chips

This variation has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 15 transcripts and has 2 individual genotypes.

Variation displays