Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.50 (T)
Location

Chromosome 12:66224858 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17826021, rs1627870

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

12:g.66224858T>C
ENST00000261233.5:c.654-1865T>C
ENST00000457197.2:c.471-1865T>C

This variation has assays on 4 chips - click the plus to show

Variation displays