Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.16 (A)
Location

Chromosome 6:6318562 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM950376

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

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

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

Variation displays