Original source

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

T/G | Ancestral: T | Ambiguity code: K | MAF: 0.42 (G)

Chromosome 4:73740952 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs3756070, rs59364491

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature, has 2557 sample genotypes and is mentioned in 16 citations.

Variant displays