Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: 0.07 (T)
Location

Chromosome 1:40368677 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.40368677A>T

Variation displays