Original source

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

Alleles
T/C/G | Ancestral: G | Ambiguity code: B | MAF: 0.25 (T)
Location

Chromosome 6:161936817 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs118125375, rs60603650

This variation has 14 HGVS names - click the plus to show

Variation displays