Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.09 (C)
Location

Chromosome 3:118201229 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17676327, rs58538112

This variation has 2 HGVS names - click the plus to show

3:g.118201229T>C
ENST00000482142.1:n.232+14241A>G

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

Variation displays