Original source

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

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

Chromosome 20:43065028 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs56973316, rs8121435

HGVS name

20:g.43065028A>C

This variation has assays on 8 chips - click the plus to show

Variation displays