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: 0.07 (T)
Location

Chromosome 11:69809714 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57025302

HGVS name

11:g.69809714C>T

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

Variation displays