Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W
Location

Chromosome 17:7184658 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

17:g.7184658A>T

Variation displays