Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

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

Most severe consequence
Evidence status


Archive dbSNP rs144609696, rs375365384

This variation has 17 HGVS names - click the plus to show

About this variant

This variant overlaps 19 transcripts and has 1093 individual genotypes.

Variation displays