Original source

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

Alleles
C/- | Ancestral: C
Location

Chromosome 1:26705452 (forward strand) | View in location tab

Co-located

with dbSNP rs9701825 (C/T)

Most severe consequence
 
Intron variant
Synonyms

Archive dbSNP rs368559809, rs199932074

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

About this variant

This variant overlaps 2 transcripts, 1 regulatory feature and has 1 sample genotype.

Variant displays