Original source

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

Alleles
-/T
Location

Chromosome 1: between 169463601 and 169463602 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs373698275, rs372958141

HGVS name

1:g.169463601_169463602insT

Variation displays