Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.49 (C)
Location

Chromosome 22:37196680 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

22:g.37196680C>T

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

Variation displays