Original source

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

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

Chromosome 2:18114553 (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.18114553A>G
ENST00000465292.1:n.305+15415A>G

Variation displays