Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.09 (G)
Location

Chromosome 1:161230796 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs59634807, rs17397854

This variation has 31 HGVS names - click the plus to show

This variation has assays on 9 chips - click the plus to show

Variation displays