Original source

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

Alleles
G/A | Ambiguity code: R | MAF: 0.07 (G)
Location

Chromosome 14:102138013 (forward strand) | View in location tab

Co-located

with dbSNP rs201102946 (G/-)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60866357, rs1742625

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

Variation displays