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: 0.43 (A)
Location

Chromosome 12:66224436 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

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

12:g.66224436A>G
ENST00000261233.5:c.654-2287A>G
ENST00000457197.2:c.471-2287A>G

This variation has assays on 7 chips - click the plus to show

Variation displays