Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 2:217342939 (forward strand) | View in location tab

Co-located

with COSMIC COSM1306416 (G/C) ; HGMD-PUBLIC CM020320 ; PhenCode SMARCAL1base_D0079:g.64512G>T (G/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 13967

This variation has 10 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays