Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.10 (T)
Location

Chromosome 1:167285547 (forward strand) | View in location tab

Co-located

with dbSNP rs67483913 (TGC/CGT)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs407668

This variant has 11 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 2507 sample genotypes.

Variant displays