Original source

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

-/ATTAT | MAF: 0.30 (-)

Chromosome 12: between 90964009 and 90964010 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs145628322

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript and has 1092 individual genotypes.

Variation displays