Original source

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

Alleles
A/- | Ancestral: A | MAF: 0.42 (A)
Location

Chromosome 1:113863923 (forward strand) | View in location tab

Co-located

with dbSNP rs66847326 (A/T)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs377767231

This variant has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts and has 2504 sample genotypes.

Variant displays