Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.37 (G)
Location

Chromosome 12:40197315 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 3 HGVS names - click the plus to show

12:g.40197315A>G
ENST00000416796.2:c.-63+542A>G
ENST00000412812.1:n.146-6921T>C

This variation has assays on 8 chips - click the plus to show

Variation displays