Original source

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

AAG/- | MAF: 0.01 (-)

Chromosome 17:58985892-58985894 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs372161170, rs140588752

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 1092 individual genotypes.

Variation displays