Original source

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

C/A | Ancestral: A | Ambiguity code: M | MAF: 0.48 (C)

Chromosome 5:1286401 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs386572964, rs59399762

HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on 13 chips - Show

About this variant

This variant overlaps 6 transcripts, has 3784 sample genotypes, is associated with 15 phenotypes and is mentioned in 121 citations.

Variant displays