Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.01 (T)
Location

Chromosome 5:151822915 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM012968

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_000171.3:c.1108G>A

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays