Original source

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

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

Chromosome 2:47804959 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM042750 ; PhenCode MMR_c.3488A>T (A/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

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

Genotyping chips

This variation has assays on: Illumina_ExomeChip, HumanCoreExome-12

Variation displays