Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

A/G/T | Ancestral: G | Ambiguity code: D | MAF: 0.38 (G)

Chromosome 12:6535556 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs116947349, rs59307765

This variation has 20 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 57 transcripts, has 1110 individual genotypes and is mentioned in 3 citations.

Variation displays