Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.30 (G)
Location

Chromosome 6:38682852 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM042995

Most severe consequence
Evidence status

Clinical significance

This variation has 11 synonyms - click the plus to show

This variation has 4 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

Variation displays