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 | MAF: 0.05 (T)
Location

Chromosome 1:156134601 (forward strand) | View in location tab

Co-located

with PhenCode LMNA:c.639+73C>T (C/T)

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

This variation has 15 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays