Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.32 (A)
Location

Chromosome 1:11796321 (forward strand) | View in location tab

Co-located

with COSMIC COSM146404 (G/A), COSM3927609 (G/A) ; HGMD-PUBLIC CM950819

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 12 HGVS names - click the plus to show

This variation has assays on 12 chips - click the plus to show

Variation displays