Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.13 (G)
Location

Chromosome 4:146637412 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

4:g.146637412C>G

About this variant

This variant overlaps 3 transcripts and has 2506 individual genotypes.

Variation displays