Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.15 (A)
Location

Chromosome 19:33989245 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3786919, rs61464660, rs253674

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

This variation has assays on 9 chips - click the plus to show

Variation displays