Original source

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

A/- | Ancestral: A | MAF: 0.09 (-)

Chromosome 15:40706105 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs141177078

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

About this variant

This variant overlaps 10 transcripts and has 1093 individual genotypes.

Variation displays