Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.41 (A)
Location

Chromosome 20:45355986 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3091927, rs57711433

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

Variation displays