Original source

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

T/G | Ancestral: G | Ambiguity code: K | MAF: 0.32 (T)

Chromosome 16:23349700 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs703780, rs61030682

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 7 transcripts and has 2775 sample genotypes.

Variant displays