Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.45 (T)
Location

Chromosome 1:12207235 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR051714

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3737956

This variation has 3 HGVS names - click the plus to show

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

Variation displays