Original source

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