Original source

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

Alleles
A/G | Ancestral: T | Ambiguity code: R | MAF: 0.18 (G)
Location

Chromosome 20:6766960 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61728311, rs61168936

HGVS name

20:g.6766960A>G

This variation has assays on 7 chips - click the plus to show

Variation displays