Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.31 (A)
Location

Chromosome 17:43044391 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs3169715, rs59800937

This variation has 5 HGVS names - click the plus to show

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

Variation displays