Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.02 (T)
Location

Chromosome 1:150670940 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58927798, rs1707159

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

About this variant

This variant overlaps 2 transcripts and has 2513 sample genotypes.

Variant displays