Original source

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

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

Chromosome 4:55130999 (forward strand) | View in location tab

Co-located

with dbSNP rs144208919 (C/-)

Most severe consequence
Evidence status

This variation has 6 HGVS names - click the plus to show

Variation displays