Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.14 (T)
Location

Chromosome 1:201327894 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.201327894C>T

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

Variation displays