Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP


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

Co-located variant

dbSNP rs386580939 (-/A)

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs78509294, rs3219202

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

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

About this variant

This variant overlaps 4 transcripts and has 44 sample genotypes.

Variant displays