Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.05 (G)
Location

Chromosome 3:159947262 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59217415

This variation has 2 HGVS names - click the plus to show

3:g.159947262A>G
ENST00000497452.2:n.1351-32788T>C

This variation has assays on 11 chips - click the plus to show

Variation displays