Original source

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

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: 0.22 (G)
Location

Chromosome 6:6143961 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

6:g.6143961T>G

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

Variation displays