Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.19 (C)
Location

Chromosome 8:72193589 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57826118, rs17710750

This variation has 11 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

Variation displays