Original source

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

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: 0.28 (A)
Location

Chromosome 1:43337449 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR043164

Most severe consequence
Evidence status

This variation has 2 HGVS names - click the plus to show

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

Variation displays