Original source

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

Alleles
G/C | Ambiguity code: S
Location

Chromosome 14:73650903 (forward strand) | View in location tab

Most severe consequence
Synonyms

Archive dbSNP rs1309160, rs1103234

This variation has 10 HGVS names - click the plus to show

Variation displays