Original source

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

Alleles
T/A | Ancestral: A | Ambiguity code: W | MAF: 0.42 (T)
Location

Chromosome 7:101323297 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59401454

HGVS name

7:g.101323297T>A

Variation displays