Original source

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

G/A/C | Ancestral: G | Ambiguity code: V | MAF: 0.30 (G)

Chromosome 12:5985679 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs5020484, rs578413, rs59667915

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and has 2514 sample genotypes.

Variant displays