Original source

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

Alleles
C/T | Ambiguity code: Y
Location

Chromosome 1:148004525 (forward strand) | View in location tab

Co-located

with dbSNP rs4067641 (A/G), rs17161529 (A/G), rs79450225 (C/T)

Most severe consequence
Evidence status

This variation has 3 HGVS names - click the plus to show

Variation displays