Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.05 (T)
Location

Chromosome 10:52771466 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920485

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 6 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 2 transcripts, has 2415 individual genotypes, is associated with 2 phenotypes and is mentioned in 55 citations.

Variation displays