Original source

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

Alleles
T/A | Ancestral: A | Ambiguity code: W | MAF: 0.49 (A)
Location

Chromosome 7:151153748 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17352673

This variant has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 2580 sample genotypes.

Variant displays