Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.26 (G)
Location

Chromosome 2:17933286 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17316374, rs61681394

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

2:g.17933286A>G
ENST00000465292.3:n.305+15415A>G

Variation displays