Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | [View in dbSNP]

Alleles
T/C | Ambiguity code: Y
Location

Chromosome 18:17484894 (forward strand) | View in location tab

Most severe consequence
Synonyms

ENSEMBL:STAR-4strain ENSRNOSNP2783225

HGVS name

18:g.17484894T>C

About this variant

This variant has 1 individual genotype.

Variation displays