Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.38 (A)
Location

Chromosome 11:69589959 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

11:g.69589959A>G
ENST00000168712.1:c.-107T>C

Variation displays