Original source

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

Alleles
C/- | Ancestral: C | MAF: 0.08 (-)
Location

Chromosome 19:42368408 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 2506 individual genotypes.

Variation displays