Original source

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

Alleles
-/T
Location

Chromosome 4: between 120055702 and 120055703 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs146386132

HGVS name

4:g.120055702_120055703insT

Variation displays