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
Location

Chromosome 1:115286135 (forward strand) | View in location tab

Co-located

with COSMIC COSM4020975 (G/A) ; HGMD-PUBLIC CM040787 ; PhenCode IPNMDB_396 (G/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

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

This variation has assays on 4 chips - click the plus to show

Variation displays