Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.01 (C)
Location

Chromosome 1:145509320 (forward strand) | View in location tab

Co-located

with dbSNP rs4032695 (C/G)

Most severe consequence
Evidence status

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

Variation displays