Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

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

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

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs144992756, rs373165846

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 2505 sample genotypes.

Variant displays