Original source

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

Alleles
G/A/T | Ancestral: G | Ambiguity code: D | MAF: 0.06 (T)
Location

Chromosome 1:156134584 (forward strand) | View in location tab

Co-located

with PhenCode LMNA:c.639+56G>T (G/T)

Most severe consequence
Evidence status

This variation has 3 synonyms - click the plus to show

This variation has 30 HGVS names - click the plus to show

Variation displays