Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.04 (C)
Location

Chromosome 22:51063477 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR890137

Most severe consequence
Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

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

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

Variation displays