Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.39 (A)
Location

Chromosome 20:22050503 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60703434, rs58031434

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

20:g.22050503A>G
ENST00000449427.1:n.342+1177A>G

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

Variation displays