Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.18 (T)
Location

Chromosome 5:131676320 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM041074

Most severe consequence
Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

This variation has 5 HGVS names - click the plus to show

This variation has assays on 11 chips - click the plus to show

Variation displays