Original source

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

Alleles
A/G/T|Ancestral: A|Ambiguity code: D|MAF: 0.01 (G)
Location

Chromosome 1:225850913 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs2090083

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 2508 sample genotypes.

Variant displays