Original source

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


Chromosome 5: between 159315986 and 159315987 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs78509294, rs3219202

This variation has 5 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 4 transcripts and has 44 individual genotypes.

Variation displays