Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.17 (T)

Chromosome 19:1222317 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs60289965

HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni2.5

About this variant

This variant overlaps 10 transcripts, 1 regulatory feature, has 3234 sample genotypes and is mentioned in 1 citation.

Variant displays