Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.20 (A)
Location

Chromosome 1:145927840 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60076035, rs17523754

This variant has 18 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

Variant displays