Original source

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

AT/- | MAF: 0.05 (-)

Chromosome 17:58993799-58993800 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs372114650, rs149614969

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

About this variant

This variant overlaps 7 transcripts and has 1092 individual genotypes.

Variation displays