Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.14 (G)
Location

Chromosome 6:161386823 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM032983

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 14 HGVS names - click the plus to show

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

Variation displays