Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W
Location

Chromosome 7:99896239 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs3179609

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 2 sample genotypes.

Variant displays