Original source

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

AC/- | MAF: 0.46 (-)

Chromosome 11:27716415-27716416 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs145592653

This variation has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 1094 individual genotypes.

Variation displays