Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.31 (A)
Location

Chromosome 1:158421044 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17627966, rs61168072

HGVS name

1:g.158421044C>A

This variation has assays on 9 chips - click the plus to show

Variation displays