Original source

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

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

Chromosome 4:120706092 (forward strand) | View in location tab

Co-located

with dbSNP rs71591574 (C/TT)

Most severe consequence

This variation has 7 HGVS names - click the plus to show

Variation displays