Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

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

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

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 2506 sample genotypes.

Variant displays