Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.46 (C)
Location

Chromosome 11:113995405 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57723843, rs1784139

This variation has 5 HGVS names - click the plus to show

This variation has assays on 6 chips - click the plus to show

Variation displays