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: 0.44 (G)
Location

Chromosome 1:55038977 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59883310, rs56641626

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

1:g.55038977G>A
LRG_275:g.4431G>A

This variation has assays on 10 chips - click the plus to show

Variation displays