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 1:204099734 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.204099734C>T

Variation displays