Original source

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

Alleles
-/T | MAF: 0.46 (-)
Location

Chromosome 16: between 22204582 and 22204583 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs148376011, rs57431613

HGVS name

16:g.22204582_22204583insT

Variation displays