Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
AA/- | MAF: < 0.01 (-)
Location

Chromosome 19:33790825-33790826 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs200218084

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

Variation displays