Original source

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

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

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs144609696, rs375365384

This variation has 10 HGVS names - click the plus to show

Variation displays