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: 0.45 (T)
Location

Chromosome 12:102399791 (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.102399791C>T
ENST00000456098.2:c.*2750G>A
ENST00000337514.7:c.*2716G>A

This variation has assays on 9 chips - click the plus to show

Variation displays