Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.01 (C)
Location

Chromosome 2:203874002 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

2:g.203874002C>T

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

Variation displays