Original source

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

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: 0.49 (T)
Location

Chromosome 6:161531855 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59792638, rs56629917

This variation has 8 HGVS names - click the plus to show

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

Variation displays