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 4:174490130 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

4:g.174490130A>T

About this variant

This variant overlaps 12 transcripts and has 231 sample genotypes.

Variant displays