Original source

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

Alleles
G/-/T
Location

Chromosome 12:11668400 (forward strand) | View in location tab

Co-located

with dbSNP rs7137918 (G/T)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs374384663

This variation has 12 HGVS names - click the plus to show

Variation displays