Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to Rnor_6.0) (release 138) | View in dbSNP

Alleles
C/T | Ambiguity code: Y
Location

Chromosome 17:49095429 (forward strand) | View in location tab

Most severe consequence
 
Intergenic variant

This variant has 2 synonyms - click the plus to show

HGVS name

17:g.49095429C>T

About this variant

This variant has 2 sample genotypes.

Variant displays