Original source

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

Alleles
G/- | Ancestral: G | MAF: 0.36 (-)
Location

Chromosome 19:49482203 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 6 HGVS names - click the plus to show

Variation displays