Original source

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

Alleles
T/C/G | Ancestral: T | Ambiguity code: B
Location

Chromosome 5:1266537 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS072295

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_198253.2:c.2583-2A>G

This variation has 16 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni5, Illumina_1M-duo

Variation displays