Original source

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

-/A | MAF: 0.18 (A)

Chromosome 16: between 74760600 and 74760601 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs79559612, rs148998226

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

About this variant

This variant overlaps 3 transcripts and has 1097 individual genotypes.

Variation displays