Original source

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

Alleles
C/-|Ancestral: C
Location

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

Co-located variant

dbSNP rs9701825 (C/T)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs368559809, rs199932074

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature and has 1 sample genotype.

Variant displays