Original source

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

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

Chromosome 1:186640638 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.186640638T>C

Variation displays