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: 0.06 (A)
Location

Chromosome 1:169467915 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs116971455, rs60335656

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

Variation displays