Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
-/T
Location

Chromosome 1: between 169432839 and 169432840 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs373698275, rs372958141

HGVS name

1:g.169432839_169432840insT

Variation displays