Original source

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

Alleles
C/A/T | Ancestral: C | Ambiguity code: H | MAF: < 0.01 (T)
Location

Chromosome 5:132385435 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM022066

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11848

This variation has 18 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip, HumanCoreExome-12

Variation displays