Original source

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

C/T | Ancestral: C | Ambiguity code: Y

Chromosome 5:68244514 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs1299759, rs1298970

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 4 transcripts and has 1 sample genotype.

Variant displays