Original source

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

C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.22 (C)

Chromosome 1:17023303 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs12750183, rs58762606

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 8 transcripts, has 3692 sample genotypes and is mentioned in 1 citation.

Variant displays