Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.06 (T)
Location

Chromosome 7:127879343 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

7:g.127879343C>T

Variation displays