Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.29 (A)
Location

Chromosome 20:44436388 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs56973316, rs8121435

HGVS name

20:g.44436388A>C

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

Variation displays