Original source

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

T/G|Ancestral: G|Ambiguity code: K|MAF: 0.03 (T)

Chromosome 2:85663648 (forward strand)|View in location tab

Co-located variant

ClinVar rs786205634 (T/-)

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs59543228

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature, has 2561 sample genotypes and is mentioned in 1 citation.

Variant displays