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 1:236755191 (forward strand) | View in location tab

Co-located

with COSMIC COSM906085 (C/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB ACTN2_2147C_T_100410

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

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays