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: 0.18 (C)
Location

Chromosome 8:31167138 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM971591

Most severe consequence
Evidence status

Clinical significance

This variation has 6 synonyms - click the plus to show

This variation has 8 HGVS names - click the plus to show

This variation has assays on 10 chips - click the plus to show

Variation displays