Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.39 (C)
Location

Chromosome 11:132012913 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59281186

This variation has 8 HGVS names - click the plus to show

11:g.132012913C>T
ENST00000374784.3:c.167+101265C>T
ENST00000479431.1:n.208+101265C>T
ENST00000374791.5:c.167+101265C>T
ENST00000498764.3:n.143+101265C>T
ENST00000550167.3:c.140+101265C>T
ENST00000374786.3:c.167+101265C>T
ENST00000425719.4:c.167+101265C>T

This variation has assays on 8 chips - click the plus to show

Variation displays