Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.31 (C)
Location

Chromosome 19:45809208 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58877977, rs17875632

HGVS name

19:g.45809208T>C

This variation has assays on 8 chips - click the plus to show

Variation displays