Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.42 (G)
Location

Chromosome 9:239313 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17719611, rs57869076

This variation has 9 HGVS names - click the plus to show

Variation displays