Original source

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

Alleles
C/- | Ancestral: C | MAF: 0.03 (-)
Location

Chromosome 1:12168975 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs377529180, rs140748620

This variation has 4 HGVS names - click the plus to show

Variation displays