Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 7:38976612 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

7:g.38976612T>G

About this variant

This variant overlaps 1 transcript.

Variant displays