Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.40 (T)
Location

Chromosome 5:157059580 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR057602

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59007920

HGVS name

5:g.157059580T>C

Variation displays