Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.01 (T)
Location

Chromosome 16:47549473 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM074412

Most severe consequence
Evidence status

Synonyms

LSDB NM_000293.2:c.555G>T

This variation has 15 HGVS names - click the plus to show

Genotyping chips

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

Variation displays