Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 1:225599113 (forward strand) | View in location tab

Co-located

with COSMIC COSM1339247 (G/A) ; HGMD-PUBLIC CM103221

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 24572

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

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays