Original source

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

Alleles
A/G | Ambiguity code: R
Location

Chromosome 17:27756502 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
HGVS name

17:g.27756502A>G

About this variant

Variant displays