Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)
Location

Chromosome 20:57899467 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM972864

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 9 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_ExomeChip, Illumina_HumanOmni5

Variation displays