Original source

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

AA/- | MAF: < 0.01 (-)

Chromosome 19:33299919-33299920 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs200218084

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

About this variant

This variant overlaps 5 transcripts and has 1092 individual genotypes.

Variation displays