Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.01 (T)
Location

Chromosome 4:120701494 (forward strand) | View in location tab

Co-located

with dbSNP rs74888165 (C/T)

Most severe consequence
Evidence status

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

Variation displays