Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

C/- | Ancestral: C | MAF: 0.07 (-)

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 2505 individual genotypes.

Variation displays