Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.09 (C)
Location

Chromosome 5:151268175 (forward strand) | View in location tab

Co-located

with dbSNP rs370553515 (G/TC)

Most severe consequence
Evidence status

This variation has 2 HGVS names - click the plus to show

Variation displays