Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.11 (T)
Location

Chromosome 11:71769952 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59349665, rs61311799

This variation has 17 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

Variation displays