Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.36 (C)
Location

Chromosome 17:63918844 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR031006

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58303360

HGVS name

17:g.63918844T>C

Variation displays