Original source

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

G/- | Ancestral: G | MAF: 0.01 (-)

Chromosome 6:143943186 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs144609696, rs375365384

HGVS names

This variant has 17 HGVS names - Show

About this variant

This variant overlaps 19 transcripts and has 2505 sample genotypes.

Variant displays