Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.04 (G)
Location

Chromosome 20:6747555 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59349630

HGVS name

20:g.6747555A>G

This variation has assays on 5 chips - click the plus to show

Variation displays