Original source

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

C/- | Ancestral: C | MAF: 0.05 (-)

Chromosome 1:169470553 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs373165846, rs144992756

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 1093 individual genotypes.

Variation displays