Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.28 (T)
Location

Chromosome 8:96161308 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs2514529

HGVS name

8:g.96161308C>T

Variation displays