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
Location

Chromosome 9:133353893 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM000442

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 7 HGVS names - click the plus to show

9:g.133353893C>T
ENST00000371974.5:c.371G>A
ENSP00000361042.3:p.Gly124Glu
ENST00000437995.1:n.317G>A
ENST00000615505.2:c.44G>A
ENSP00000482067.1:p.Gly15Glu
ENST00000495952.3:n.361G>A

Genotyping chips

This variation has assays on: Illumina_Human1M-duo

Variation displays