Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: < 0.01 (G)
Location

Chromosome 1:97082275 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs473113, rs291600

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

This variation has assays on 5 chips - click the plus to show

Variation displays