Original source

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

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

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

Co-located variant

dbSNP rs66847326 (A/T)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs377767231

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 11 transcripts and has 2504 sample genotypes.

Variant displays