Original source

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

Alleles
G/A/C | Ancestral: G | Ambiguity code: V | MAF: 0.01 (A)
Location

Chromosome 7:44149794 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM004359

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB GCK_645C_G_112910

This variation has 17 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays