Original source

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

Alleles
T/- | Ancestral: T
Location

Chromosome 4:120706086 (forward strand) | View in location tab

Co-located

with dbSNP rs75046371 (T/C)

Most severe consequence
Evidence status

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

Variation displays