Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.45 (C)
Location

Chromosome 1:67753508 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58127206

HGVS name

1:g.67753508C>T

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

Variation displays