Original source

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

Alleles
C/- | Ancestral: C | MAF: 0.04 (-)
Location

Chromosome 1:12168975 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs377529180, rs140748620

This variant has 4 HGVS names - click the plus to show

About this variant

Variant displays