Original source

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

Alleles
G/A | Ambiguity code: R | MAF: 0.16 (T)
Location

Chromosome 1:149033329 (forward strand) | View in location tab

Co-located

with dbSNP rs72633604 (G/A)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61804965

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

Variation displays