Original source

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

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

Chromosome 6:161952887 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59792638, rs56629917

This variation has 7 HGVS names - click the plus to show

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

Variation displays