Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y
Location

Chromosome 14:74902643 (forward strand) | View in location tab

Co-located

with dbSNP rs11548706 (C/T)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3199989, rs61044770

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

Variation displays