Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.20 (T)
Location

Chromosome 12:66209619 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

12:g.66209619C>T
ENST00000261233.6:c.381+99C>T
ENST00000457197.2:c.198+99C>T

Variation displays