Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: < 0.01 (T)
Location

Chromosome 19:14729592 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

19:g.14729592C>T

Variation displays