Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.37 (A)
Location

Chromosome 22:19963748 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM960420

Most severe consequence
Evidence status

Clinical significance

This variation has 16 synonyms - click the plus to show

This variation has 20 HGVS names - click the plus to show

This variation has assays on 14 chips - click the plus to show

About this variant

This variant overlaps 12 transcripts, has 4403 individual genotypes, is associated with 3 phenotypes and is mentioned in 478 citations.

Variation displays