Original source

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

G/T | Ancestral: G | Ambiguity code: K | MAF: 0.50 (G)

Chromosome 7:44182404 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs61340685

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5, Illumina_Cardio-Metabo_Chip

About this variant

This variant overlaps 3 transcripts and has 2657 sample genotypes.

Variant displays