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: 0.29 (T)
Location

Chromosome 2:17933665 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR052973

Most severe consequence
Evidence status

This variation has 2 HGVS names - click the plus to show

2:g.17933665C>T
ENST00000465292.2:n.305+15794C>T

Genotyping chips

This variation has assays on: Illumina_HumanHap650Y, Illumina_1M-duo

Variation displays