Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.37 (G)
Location

Chromosome 22:19150659 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

22:g.19150659C>G

About this variant

This variant overlaps 1 transcript and has 2505 individual genotypes.

Variation displays