Original source

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

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

Chromosome 2:47800616 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM003461 ; PhenCode MMR_c.2633T>C (T/C)

Most severe consequence
Evidence status

Clinical significance

This variation has 7 synonyms - click the plus to show

This variation has 18 HGVS names - click the plus to show

This variation has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 15 transcripts, has 1807 individual genotypes, is associated with 6 phenotypes and is mentioned in 6 citations.

Variation displays