Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs373165846, rs144992756

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

About this variant

This variant overlaps 3 transcripts and has 2505 sample genotypes.

Variant displays