Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.48 (C)

Chromosome 12:6042707 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs644044, rs216786, rs58546313

This variation has 3 HGVS names - click the plus to show

This variation has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 2316 individual genotypes.

Variation displays